Table of Contents

 
UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
Form 10-Q
þQUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended September 30, 2016March 31, 2017
OR
¨TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from_____________to___________                 

Commission File Number 333-199861
MYLAN N.V.
(Exact name of registrant as specified in its charter)
The Netherlands 98-1189497
(State or other jurisdiction
of incorporation or organization)
 
(I.R.S. Employer
Identification No.)
Building 4, Trident Place, Mosquito Way, Hatfield, Hertfordshire, AL10 9UL, England
(Address of principal executive offices)
+44 (0) 1707-853-000
(Registrant’s telephone number, including area code)
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.    Yes  þ    No  ¨
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).    Yes  þ    No  ¨
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer”filer,” “smaller reporting company,” and “smaller reporting“emerging growth company” in Rule 12b-2 of the Exchange Act. (Check one):
Large accelerated filer þ Accelerated filer ¨
       
Non-accelerated filer 
¨  (Do not check if a smaller reporting company)
 Smaller reporting company ¨
Emerging growth company¨
If an emerging growth company, indicate by check mark if the registrant has elected not to us the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).    Yes  ¨    No  þ
Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date.

As of NovemberMay 4, 2016,2017, there were 535,105,253535,950,491 of the issuer’s €0.01 nominal value ordinary shares outstanding.

 

MYLAN N.V. AND SUBSIDIARIES
INDEX TO FORM 10-Q
For the Quarterly Period Ended
September 30, 2016March 31, 2017
 

  
 Page
 PART I — FINANCIAL INFORMATION 
ITEM 1.Condensed Consolidated Financial Statements (unaudited) 
 
 
 
 
   
 
   
ITEM 2.
   
ITEM 3.
   
ITEM 4.
   
 PART II — OTHER INFORMATION 
ITEM 1.
   
ITEM 1A.
   
ITEM 6.
   
 

PART I — FINANCIAL INFORMATION


MYLAN N.V. AND SUBSIDIARIES
Condensed Consolidated Statements of Operations
(Unaudited; in millions, except per share amounts)
Three Months Ended Nine Months EndedThree Months Ended
September 30, September 30,March 31,
2016 2015 2016 20152017 2016
Revenues:          
Net sales$3,029.5
 $2,676.2
 $7,745.5
 $6,887.8
$2,687.4
 $2,176.1
Other revenues27.6
 19.0
 63.6
 50.8
32.1
 15.2
Total revenues3,057.1
 2,695.2
 7,809.1
 6,938.6
2,719.5
 2,191.3
Cost of sales1,773.8
 1,379.9
 4,447.1
 3,785.1
1,634.5
 1,284.3
Gross profit1,283.3
 1,315.3
 3,362.0
 3,153.5
1,085.0
 907.0
Operating expenses:          
Research and development199.1
 174.8
 632.2
 512.9
217.5
 253.6
Selling, general and administrative656.9
 537.1
 1,787.6
 1,584.5
631.3
 549.3
Litigation settlements and other contingencies, net558.0
 2.3
 556.4
 19.1
9.0
 (1.5)
Total operating expenses1,414.0
 714.2
 2,976.2
 2,116.5
857.8
 801.4
(Loss) earnings from operations(130.7) 601.1
 385.8
 1,037.0
Earnings from operations227.2
 105.6
Interest expense144.4
 95.1
 305.0
 268.5
138.2
 70.3
Other expense, net50.2
 50.9
 184.0
 71.4
17.4
 16.3
(Loss) earnings before income taxes and noncontrolling interest(325.3) 455.1
 (103.2) 697.1
Income tax (benefit) provision(205.5) 26.5
 (165.7) 44.0
Net (loss) earnings(119.8) 428.6
 62.5
 653.1
Net earnings attributable to the noncontrolling interest
 
 
 (0.1)
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders$(119.8) $428.6
 $62.5
 $653.0
(Loss) earnings per ordinary share attributable to Mylan N.V. ordinary shareholders:       
Earnings before income taxes71.6
 19.0
Income tax provision5.2
 5.1
Net earnings$66.4
 $13.9
Earnings per ordinary share:   
Basic$(0.23) $0.87
 $0.12
 $1.40
$0.12
 $0.03
Diluted$(0.23) $0.83
 $0.12
 $1.32
$0.12
 $0.03
Weighted average ordinary shares outstanding:          
Basic523.6
 490.5
 505.9
 466.2
534.5
 489.8
Diluted523.6
 514.0
 515.2
 493.2
536.9
 509.6



See Notes to Condensed Consolidated Financial Statements
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Table of Contents

MYLAN N.V. AND SUBSIDIARIES
Condensed Consolidated Statements of Comprehensive Earnings
(Unaudited; in millions)
 Three Months Ended Nine Months Ended
 September 30, September 30,
 2016 2015 2016 2015
        
Net (loss) earnings$(119.8) $428.6
 $62.5
 $653.1
Other comprehensive earnings (loss), before tax:       
Foreign currency translation adjustment290.6
 (148.4) 645.5
 (526.7)
Change in unrecognized gain (loss) and prior service cost related to defined benefit plans0.1
 
 (0.3) 3.9
Net unrecognized gain (loss) on derivatives in cash flow hedging relationships22.8
 (84.2) (22.9) (67.4)
Net unrecognized loss on derivatives in net investment hedging relationships(10.4) 
 (10.4) 
Net unrealized gain (loss) on marketable securities21.5
 (0.2) 32.5
 (0.4)
Other comprehensive earnings (loss), before tax324.6
 (232.8) 644.4
 (590.6)
Income tax provision (benefit)13.7
 (30.8) 0.5
 (24.0)
Other comprehensive earnings (loss), net of tax310.9
 (202.0) 643.9
 (566.6)
Comprehensive earnings191.1
 226.6
 706.4
 86.5
Comprehensive earnings attributable to the noncontrolling interest
 
 
 (0.1)
Comprehensive earnings attributable to Mylan N.V. ordinary shareholders$191.1
 $226.6
 $706.4
 $86.4
 Three Months Ended
 March 31,
 2017 2016
Net earnings$66.4
 $13.9
Other comprehensive earnings (loss), before tax:   
Foreign currency translation adjustment434.2
 502.0
Change in unrecognized loss and prior service cost related to defined benefit plans
 (0.3)
Net unrecognized gain (loss) on derivatives in cash flow hedging relationships32.4
 (49.1)
Net unrecognized loss on derivatives in net investment hedging relationships(9.9) 
Net unrealized gain on marketable securities7.7
 4.4
Other comprehensive earnings, before tax464.4
 457.0
Income tax provision (benefit)13.7
 (16.8)
Other comprehensive earnings, net of tax450.7
 473.8
Comprehensive earnings$517.1
 $487.7




See Notes to Condensed Consolidated Financial Statements
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Table of Contents

MYLAN N.V. AND SUBSIDIARIES
Condensed Consolidated Balance Sheets
(Unaudited; in millions, except share and per share amounts)
September 30,
2016
 December 31,
2015
March 31,
2017
 December 31,
2016
ASSETS
Assets      
Current assets:      
Cash and cash equivalents$1,256.6
 $1,236.0
$723.8
 $998.8
Accounts receivable, net3,098.9
 2,689.1
2,872.0
 3,310.9
Inventories2,687.5
 1,951.0
2,547.8
 2,456.4
Prepaid expenses and other current assets922.1
 596.6
921.9
 756.4
Total current assets7,965.1
 6,472.7
7,065.5
 7,522.5
Property, plant and equipment, net2,284.2
 1,983.9
2,338.0
 2,322.2
Intangible assets, net15,613.4
 7,221.9
14,370.0
 14,447.8
Goodwill9,633.1
 5,380.1
9,394.1
 9,231.9
Deferred income tax benefit441.8
 457.6
564.0
 633.2
Other assets600.9
 751.5
541.0
 568.6
Total assets$36,538.5
 $22,267.7
$34,272.6
 $34,726.2
      
LIABILITIES AND EQUITY
Liabilities      
Current liabilities:      
Trade accounts payable$1,254.9
 $1,109.6
$1,141.4
 $1,348.1
Short-term borrowings54.2
 1.3
31.0
 46.4
Income taxes payable164.5
 92.4
31.0
 97.7
Current portion of long-term debt and other long-term obligations4,434.6
 1,077.0
294.4
 290.0
Other current liabilities3,645.8
 1,841.9
3,026.4
 3,258.5
Total current liabilities9,554.0
 4,122.2
4,524.2
 5,040.7
Long-term debt11,328.6
 6,295.6
14,700.8
 15,202.9
Deferred income tax liability2,189.6
 718.1
2,019.1
 2,006.4
Other long-term obligations1,637.5
 1,366.0
1,372.5
 1,358.6
Total liabilities24,709.7
 12,501.9
22,616.6
 23,608.6
Equity      
Mylan N.V. shareholders’ equity      
Ordinary shares — nominal value €0.01 per ordinary share      
Shares authorized: 1,200,000,000      
Shares issued: 536,384,447 and 491,928,095 as of September 30, 2016 and December 31, 20156.0
 5.5
Shares issued: 537,237,925 and 536,639,291 as of March 31, 2017 and December 31, 20166.0
 6.0
Additional paid-in capital8,484.6
 7,128.6
8,522.0
 8,499.3
Retained earnings4,524.6
 4,462.1
5,008.5
 4,942.1
Accumulated other comprehensive loss(1,120.4) (1,764.3)(1,813.0) (2,263.7)
11,894.8
 9,831.9
11,723.5
 11,183.7
Noncontrolling interest1.5
 1.4

 1.4
Less: Treasury stock — at cost
  
  
Shares: 1,311,193 as of September 30, 2016 and December 31, 201567.5
 67.5
Ordinary shares: 1,311,193 as of March 31, 2017 and December 31, 201667.5
 67.5
Total equity11,828.8
 9,765.8
11,656.0
 11,117.6
Total liabilities and equity$36,538.5
 $22,267.7
$34,272.6
 $34,726.2
      


See Notes to Condensed Consolidated Financial Statements
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MYLAN N.V. AND SUBSIDIARIES
Condensed Consolidated Statements of Cash Flows
(Unaudited; in millions)
Nine Months EndedThree Months Ended
September 30,March 31,
2016 20152017 2016
Cash flows from operating activities:      
Net earnings$62.5
 $653.1
$66.4
 $13.9
Adjustments to reconcile net earnings to net cash provided by operating activities:      
Depreciation and amortization1,046.4
 691.4
415.5
 297.1
Share-based compensation expense71.1
 66.4
23.1
 26.5
Deferred income tax benefit(356.6) (62.2)
Deferred income tax expense35.6
 38.5
Loss from equity method investments85.5
 77.5
33.2
 30.9
Other non-cash items226.1
 206.2
98.8
 81.0
Litigation settlements and other contingencies, net558.6
 19.1
8.9
 0.3
Write off of financing fees35.8
 
Losses on acquisition-related foreign currency derivatives128.6
 
Changes in operating assets and liabilities:      
Accounts receivable183.3
 (54.3)286.7
 83.5
Inventories(336.7) (288.4)(105.6) (222.8)
Trade accounts payable(45.0) 242.5
(242.7) (57.2)
Income taxes51.3
 (178.5)(175.0) (84.7)
Other operating assets and liabilities, net(13.2) (16.3)8.0
 (126.5)
Net cash provided by operating activities1,697.7
 1,356.5
452.9
 80.5
Cash flows from investing activities:      
Cash paid for acquisitions, net(71.6) 
Capital expenditures(239.5) (207.3)(58.4) (51.8)
Proceeds from sale of assets31.1
 
Change in restricted cash(50.5) 25.9
12.7
 
Purchase of marketable securities(22.8) (59.1)(2.3) (8.5)
Proceeds from sale of marketable securities15.8
 29.4
2.3
 5.9
Cash paid for acquisitions, net(6,151.7) 
Cash paid for Meda's unconditional deferred payment(308.0) 
Settlement of acquisition-related foreign currency derivatives(128.6) 
Payments for product rights and other, net(196.3) (428.2)(77.9) (105.6)
Net cash used in investing activities(7,081.6) (639.3)(164.1) (160.0)
Cash flows from financing activities:      
Payments of financing fees(95.3) (114.7)
Payments of long-term debt(550.0) 
Change in short-term borrowings, net48.6
 (329.7)(17.6) 65.1
Proceeds from convertible note hedge
 1,970.8
Proceeds from issuance of long-term debt6,519.8
 2,390.0
Payments of long-term debt(1,067.0) (4,334.1)
Proceeds from exercise of stock options11.1
 92.8
Taxes paid related to net share settlement of equity awards(12.9) (31.7)(6.1) (6.9)
Contingent consideration payments(15.5) 
(3.8) 
Acquisition of noncontrolling interest(1.0) (11.7)
Payments of financing fees(3.7) (31.6)
Proceeds from exercise of stock options5.0
 3.6
Other items, net1.6
 49.6
0.5
 0.3
Net cash provided by (used in) financing activities5,389.4
 (318.7)
Net cash (used in) provided by financing activities(575.7) 30.5
Effect on cash of changes in exchange rates15.1
 (37.0)11.9
 12.4
Net increase in cash and cash equivalents20.6
 361.5
Net decrease in cash and cash equivalents(275.0) (36.6)
Cash and cash equivalents — beginning of period1,236.0
 225.5
998.8
 1,236.0
Cash and cash equivalents — end of period$1,256.6
 $587.0
$723.8
 $1,199.4
Supplemental disclosures of cash flow information —   
Non-cash transactions:   
Ordinary shares issued for acquisition$1,281.7
 $6,305.8

See Notes to Condensed Consolidated Financial Statements
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Table of Contents
MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited)


1.General
The accompanying unaudited Condensed Consolidated Financial Statements (“interim financial statements”) of Mylan N.V. and subsidiaries (“Mylan” or the “Company”) were prepared in accordance with accounting principles generally accepted in the United States of America (“U.S. GAAP”) and the rules and regulations of the U.S. Securities and Exchange Commission (the “SEC”) for reporting on Form 10-Q; therefore, as permitted under these rules, certain footnotes and other financial information included in audited financial statements were condensed or omitted. The interim financial statements contain all adjustments (consisting of only normal recurring adjustments) necessary to present fairly the interim results of operations, comprehensive earnings, financial position and cash flows for the periods presented. For periods prior to February 27, 2015, the Company’s interim financial statements present the accounts of Mylan Inc. and subsidiaries.
These interim financial statements should be read in conjunction with the Consolidated Financial Statements and Notes thereto in Mylan N.V.’s Annual Report on Form 10-K for the year ended December 31, 20152016, as amended. The December 31, 20152016 Condensed Consolidated Balance Sheet was derived from audited financial statements.
The interim results of operations, and comprehensive earnings for the three and nine months ended September 30, 2016 and cash flows for the ninethree months ended September 30, 2016March 31, 2017 are not necessarily indicative of the results to be expected for the full fiscal year or any other future period.
2.Revenue Recognition and Accounts Receivable
The Company recognizes net sales when title and risk of loss pass to its customers and when provisions for estimates, including discounts, sales allowances, price adjustments, returns, chargebacks and other promotional programs are reasonably determinable.
Accounts receivable are presented net of allowances relating to these provisions. No significant revisions were made to the methodology used in determining these provisions or the nature of the provisions during the ninethree months ended September 30, 2016.March 31, 2017. Such allowances were $1.83$2.14 billion and $1.84$2.05 billion at September 30, 2016March 31, 2017 and December 31, 2015,2016, respectively. Other current liabilities include $824.1$616.5 million and $681.8$809.0 million at September 30, 2016March 31, 2017 and December 31, 2015,2016, respectively, for certain sales allowances and other adjustments that are paid to customers.settled in cash.
Accounts receivable, net was comprised of the following at March 31, 2017 and December 31, 2016, respectively:
(In millions)March 31,
2017
 December 31,
2016
Trade receivables, net$2,568.2
 $3,015.4
Other receivables303.8
 295.5
Accounts receivable, net$2,872.0
 $3,310.9
Through its wholly owned subsidiary Mylan Pharmaceuticals Inc. (“MPI”), the Company has access to a $400 million accounts receivable securitization facility (the “Receivables Facility”). The receivables underlying any borrowings are included in accounts receivable, net, in the Condensed Consolidated Balance Sheets. There were $759.3854.8 million and $914.2 million$1.13 billion of securitized accounts receivable at September 30, 2016March 31, 2017 and December 31, 20152016, respectively.
3.Recent Accounting Pronouncements
In October 2016,March 2017, the Financial Accounting Standards Board (“FASB”(the “FASB”) issued Accounting Standards Update 2016-16,2017-07, Income TaxesCompensation - Retirement Benefits (Topic 740)715): Improving the Presentation of Net Periodic Pension Cost and Net Periodic Postretirement Benefit Cost (“ASU 2016-16”2017-07”), which reducesrequires companies to disaggregate the complexityservice cost component from the other components of net benefit cost and disclose the amount of net benefit cost that is included in the accounting standardsincome statement or capitalized in assets, by allowingline item. This guidance requires companies to report the recognitionservice cost component in the same line item(s) as other compensation costs and to report other pension-related costs (which include interest costs, amortization of currentpension-related costs from prior periods and deferredgains or losses on plan assets) separately and exclude them from the subtotal of operating income. This guidance also allows only the service cost component to be eligible for capitalization when applicable. This guidance is effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2017. This guidance should be applied retrospectively for the presentation of the service cost component and the

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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


other components of net periodic pension cost and net periodic postretirement benefit cost in the income taxesstatement and prospectively, on and after the effective date, for the capitalization of the service cost component of net periodic pension cost and net periodic postretirement benefit in assets. The update allows a practical expedient that permits a company to use the amounts disclosed in its pension and other postretirement plan note for the prior comparative periods as the estimation basis for applying the retrospective presentation requirements. The Company is currently assessing the impact of the adoption of this guidance on its consolidated financial statements and disclosures.
In January 2017, the FASB issued Accounting Standards Update 2017-04, Intangibles - Goodwill and Other (Topic 350): Simplifying the Test for Goodwill Impairment (“ASU 2017-04”), which simplifies the subsequent measurement of goodwill by eliminating Step 2 from the goodwill impairment test which previously required measurement of any goodwill impairment loss by comparing the implied fair value of a reporting unit’s goodwill with the carrying amount of that goodwill. Under ASU 2017-04, an intra-entityentity should perform its annual, or interim, goodwill impairment test by comparing the fair value of a reporting unit with its carrying value and recognize an impairment charge for the amount by which the carrying amount exceeds the reporting unit’s fair value; without exceeding the total amount of goodwill allocated to that reporting unit. This guidance is effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2019, with early adoption permitted. The Company has elected to early adopt this guidance as of January 1, 2017 and will apply it on a prospective basis. The adoption did not have a material impact on its condensed consolidated financial statements.
In January 2017, the FASB issued Accounting Standards Update 2017-01, Business Combinations (Topic 805) Clarifying the Definition of a Business (“ASU 2017-01”), which narrows the definition of a business and requires an entity to evaluate if substantially all of the fair value of the gross assets acquired is concentrated in a single identifiable asset transfer, other than inventory, whenor a group of similar identifiable assets, which would not constitute the transfer occurs.acquisition of a business. The guidance also requires a business to include at least one substantive process and narrows the definition of outputs. This guidance is effective for fiscal years beginning after December 15, 2017, and interim periods within those fiscal years, with early adoption permitted using a modified retrospective transition approach.permitted. The Company is currently assessing the impact of the adoption ofhas elected to early adopt this guidance as of January 1, 2017 and will apply it on a prospective basis. The adoption did not have a material impact on its condensed consolidated financial statements and disclosures.
In August 2016, the FASB issued Accounting Standards Update 2016-15, Statement of Cash Flows (Topic 230) (“ASU 2016-15”), which clarifies how certain cash receipts and cash payments should be presented in the Statement of Cash Flows. This guidance is effective for fiscal years beginning after December 15, 2017, and interim periods within those fiscal years, with early adoption permitted using a retrospective transition approach. The Company is currently assessing the impact of the adoption of this guidance on its Statement of Cash Flows.statements.
In March 2016, the FASB issued Accounting Standards Update 2016-09, Compensation - Stock Compensation (Topic 718) (“ASU 2016-09”), which simplifies the accounting for share-based compensation payments. The new standard requires all excess tax benefits and tax deficiencies (including tax benefits of dividends on share-based payment awards) to be recognized as income tax expense or benefit on the income statement. The tax effects of exercised or vested awards should be treated as discrete items in the reporting period in which they occur. This guidance is effective for fiscal years,ASU 2016-09 also addresses the classification of excess tax benefits in the statement of cash flows. As required, the Company applied the provisions of ASU 2016-09 on a prospective basis as of January 1, 2017 and interim periods within

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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


those years, beginning after December 15, 2016, with early adoption permitted. The Company is currently assessing the impact of the adoption of this guidancedid not have a material impact on its condensed consolidated financial statements and disclosures.
In February 2016, the FASB issued Accounting Standards Update 2016-02, Leases (Topic 840) (“ASU 2016-02”), which provides principles for the recognition, measurement, presentation and disclosure of leases for both lessees and lessors. The new standard requires lessees to apply a dual approach, classifying leases as either finance or operating leases based on the principle of whether or not the lease is effectively a financed purchase by the lessee. This classification will determine whether lease expense is recognized based on an effective interest method or on a straight-line basis over the term of the lease. A lessee is also required to record a right-of-use asset and a lease liability for all leases with a term of greater than twelve months regardless of classification. Leases with a term of twelve months or less will be accounted for similar to existing guidance for operating leases. This guidance is effective for annual and interim periods beginning after December 15, 2018, with early adoption permitted. The Company is currently assessing the impact of the adoption of this guidance on its consolidated financial statements and disclosures.
In January 2016, the FASB issued Accounting Standards Update 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities (“ASU 2016-01”), which requires that most equity investments be measured at fair value, with subsequent changes in fair value recognized in net income (other than those accounted for under equity method of accounting). The amendments in this update also require an entity to present separately in other comprehensive earnings the portion of the total change in the fair value of a liability resulting from a change in the instrument-specific credit risk when the entity has elected to measure the liability at fair value in accordance with the fair value option for financial instruments. ASU 2016-01 also impacts financial liabilities under the fair value option and the presentation and disclosure requirements for financial instruments. This guidance is effective for fiscal years, and interim periods within those years, beginning after December 15, 2017. The Company is currently assessing the impact of the adoption of this guidance on its consolidated financial statements and disclosures.statements.
In May 2014, the FASB issued Accounting Standards Update 2014-09, Revenue from Contracts with Customers (“ASU 2014-09” updated with “ASU 2015-14”, “ASU 2016-08”, “ASU 2016-10”, “ASU 2016-12” and “ASU 2016-12”2016-20”), which revises accounting guidance on revenue recognition that will supersede nearly all existing revenue recognition guidance under U.S. GAAP. The core principal of this guidance is that an entity should recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. This guidance also requires additional disclosure about the nature, amount, timing and uncertainty of revenue and cash flows arising from customer contracts, including significant judgments and changes in judgments and assets recognized from costs incurred to obtain or fulfill a contract. This guidance is effective for fiscal years beginning after December 15, 2017, and for interim periods within those fiscal years, and can be applied using a full retrospective or modified retrospective approach. The Company continues to review specific revenue arrangements, including customer and collaboration contracts, and expects to complete the review in the third quarter of 2017. The Company is currently assessing the impact ofstill evaluating the adoption of this guidance on its consolidated financial statements and disclosures.method it will elect upon implementation.
4.Acquisitions and Other Transactions
Meda AB
On February 10, 2016, the Company issued an offer announcement under the Nasdaq Stockholm’s Takeover Rules and the Swedish Takeover Act (collectively, the “Swedish Takeover Rules”) setting forth a public offer to the shareholders of Meda AB (publ.) (“Meda”) to acquire all of the outstanding shares of Meda (the “Offer”), with an enterprise value, including the net debt of Meda, of approximately Swedish kronor (“SEK” or “kr”) 83.6 billion (based on a SEK/USD exchange rate of 8.4158) or $9.9 billion at announcement. On August 2, 2016, the Company announced that the Offer was accepted by Meda

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shareholders holding an aggregate of approximately 343 million shares, representing approximately 94% of the total number of outstanding Meda shares, as of July 29, 2016, and the Company declared the Offer unconditional. On August 5, 2016, settlement occurred with respect to the Meda shares duly tendered by July 29, 2016 and, as a result, Meda is nowbecame a controlled subsidiary of the Company. Pursuant to the terms of the Offer, each Meda shareholder that duly tendered Meda shares into the Offer received at settlement (1) in respect of 80% of the number of Meda shares tendered by such shareholder, 165kr in cash per Meda share, and (2) in respect of the remaining 20% of the number of Meda shares tendered by such shareholder, 0.386 of the Company’s ordinary shares per Meda share (subject to treatment of fractional shares as described in the offer document published on June 16, 2016). The non-tendered shares willwere required to be acquired for cash through a compulsory acquisition proceeding, in accordance with the Swedish Companies Act (Sw. aktiebolagslagen (2005:551)), with advance title to such non-tendered shares expected to be acquired within six to twelve months of the acquisition date.. The compulsory acquisition proceeding price will accrueaccrued interest as required by the Swedish Companies Act. Meda’s shares were delisted from the Nasdaq Stockholm

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exchange on August 23, 2016.
On November 1, 2016, the Company made an offer to the remaining Meda shareholders to tender all their Meda shares for cash consideration of 161.31kr per Meda share (the “November Offer”) to provide such remaining shareholders with an opportunity to sell their shares in Meda to the Company in advance of the automatic acquisition of their shares for cash in connection with the compulsory acquisition proceeding. The acceptance periodAt the end of November 2016, Mylan completed the acquisition of approximately 19 million Meda shares duly tendered for aggregate cash consideration of approximately $330.3 million. In March 2017, the November Offer expires on November 23, 2016 and settlement is expectedCompany received full legal ownership to occur on or around November 30, 2016.the remaining non-tendered Meda shareholders who tender their shares in the November Offer will not have the right to withdraw their acceptances, and there are no conditionsexchange for a cash payment of approximately $71.6 million, equal to the completionuncontested portion of the November Offer. Any Meda shareholders that do not accept the November Offer will automatically receive all-cash considerationcompulsory acquisition price plus statutory interest, for theirand the Company’s arrangement of a customary bank guarantee to secure the payment of any additional cash consideration that may be awarded to the former Meda shares as determinedshareholders in the compulsory acquisition proceeding. The November Offer is not being made, nor will any tender of shares be accepted from or on behalf of holders in, any jurisdiction in which the making of the November Offer or the acceptance of any tender of shares would contravene applicable laws or regulations or require any offer documents, filings or other measures. In connection with either the November Offer orarbitration tribunal conducting the compulsory acquisition proceeding it has been assumed thatwill determine whether to award any such additional cash consideration at the fair valuecompletion of the non-tendered sharescompulsory acquisition proceeding, which is currently expected to occur in 2017 or 2018. As of March 31, 2017, the Company continues to maintain the bank guarantee as required by Swedish law. The Company does not expect that any additional payments in connection with the compulsory acquisition proceeding would be approximately 161kr per share at settlement.material to the consolidated financial statements.
TheOn August 5, 2016, the total purchase price was approximately $6.92 billion, net of cash acquired, which includes cash consideration paid of approximately $5.3 billion, the issuance of approximately 26.4 million Mylan N.V. ordinary shares at a fair value of approximately $1.3 billion based on the closing price of the Company’s ordinary shares on August 5, 2016, as reported by the NASDAQ Global Select Stock Market (the “NASDAQ”(“NASDAQ”) and an assumed liability of approximately $431.0 million related to the November Offer and the compulsory acquisition proceeding offor the non-tendered Meda shares, which is classified as a current liability on the Condensed Consolidated Balance Sheet.shares. In accordance with U.S. GAAP, the Company used the acquisition method of accounting to account for this transaction. Under the acquisition method of accounting, the assets acquired and liabilities assumed in the transaction have been recorded at their respective estimated fair values at the acquisition date. Acquisition related costs of approximately $65.8 million and $212.5 million were incurred during
During the three and nine months ended September 30, 2016, respectively, whichMarch 31, 2017, adjustments were recordedmade to the preliminary purchase price and are reflected as components of research and development expense (“R&D”), selling, general and administrative expense (“SG&A”), interest expense and other expense, net“Measurement Period Adjustments” in the Condensed Consolidated Statements of Operations. For the three and nine months ended September 30, 2016, these costs include approximately $44.4 million and $128.6 million, respectively, of losses on non-designated foreign currency forward and option contracts entered into in order to economically hedge the SEK purchase price of the Offer (explained further in Note 11Financial Instruments and Risk Management). For the nine months ended September 30, 2016 acquisition related costs include approximately $45.2 million of financing fees related to the terminated 2016 Bridge Credit Agreement (explained further in Note 12Debt).
table below. The preliminary allocation of the $6.92 billion purchase price to the assets acquired and liabilities assumed for Meda is as follows:

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(In millions) 
Current assets (excluding inventories and net of cash acquired)$470.2
Inventories465.7
Property, plant and equipment177.5
Identified intangible assets8,060.7
Goodwill3,677.6
Other assets9.3
Total assets acquired12,861.0
Current liabilities(1,088.4)
Long-term debt, including current portion(2,864.6)
Deferred tax liabilities(1,628.1)
Pension and other postretirement benefits(322.3)
Other noncurrent liabilities(36.5)
Net assets acquired$6,921.1

(In millions)
Preliminary Purchase Price Allocation as of December 31, 2016 (a)
 
Measurement Period Adjustments (b)
 Preliminary Purchase Price Allocation as of March 31, 2017 (as adjusted)
Current assets (excluding inventories and net of cash acquired)$482.5
 $
 $482.5
Inventories463.1
 
 463.1
Property, plant and equipment177.5
 
 177.5
Identified intangible assets8,060.7
 
 8,060.7
Goodwill3,676.9
 1.7
 3,678.6
Other assets9.5
 
 9.5
Total assets acquired12,870.2
 1.7
 12,871.9
Current liabilities(1,105.9) 
 (1,105.9)
Long-term debt, including current portion(2,864.6) 
 (2,864.6)
Deferred tax liabilities(1,613.9) (1.7) (1,615.6)
Pension and other postretirement benefits(322.3) 
 (322.3)
Other noncurrent liabilities(42.4) 
 (42.4)
Net assets acquired$6,921.1
 $
 $6,921.1
____________
(a)
As previously reported in the Company’s December 31, 2016 Annual Report on Form 10-K, as amended.
(b)
The measurement period adjustments were recorded in the first quarter of 2017 and are primarily related to certain income tax adjustments to reflect facts and circumstances that existed as of the acquisition date.
The preliminary fair value estimates for the assets acquired and liabilities assumed were based upon preliminary calculations, valuations and assumptions that are subject to change as the Company obtains additional information during the

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measurement period (up to one year from the acquisition date). The primary areas subject to change relate to the finalization of the working capital components the valuation of intangible assets and income taxes.
The acquisition of Meda createscreated a more diversified and expansive portfolio of branded and generic medicines along with a strong and growing portfolio of over-the-counter (“OTC”) products. The combined company has a balanced global footprint with significant scale in key geographic markets, particularly the U.S. and Europe. The acquisition of Meda also provides Mylan with entry into a number of new and attractiveexpanded our presence in emerging markets, including China, Southeastwhich includes countries in Africa, as well as countries throughout Asia Russia,and the Middle East, and Mexico,is complemented by Mylan’s presence in India, Brazil and Africa.Africa (including South Africa). The Company recorded a step-up in the fair value of inventory of approximately $107 million. Duringmillion at the three and nine months ended September 30, 2016, the Company recorded amortizationacquisition date, which was fully amortized as of the inventory step-up of approximately $42.8 million, which is included in cost of sales in the Condensed Consolidated Statements of Operations.December 31, 2016.
The identified intangible assets of $8.06 billion are comprised of product rights and licenses that have a weighted average useful life of 20 years. Significant assumptions utilized in the valuation of identified intangible assets were based on company specific information and projections which are not observable in the market and are thus considered Level 3 measurements as defined by U.S. GAAP. The goodwill of $3.68 billion arising from the acquisition consisted largely of the value of the employee workforce and the expected value of products to be developed in the future. The newly acquired operations havefinal allocation of goodwill to Mylan’s reportable segments has not been included incompleted; however, the Generics segment for the three and nine months ended September 30, 2016. In addition, allmajority of the goodwill was assignedis expected to be allocated to the GenericsEurope segment. None of the goodwill recognized in this transaction is currently expected to be deductible for income tax purposes.
The settlement of the Offer constituted an Acceleration Event (as defined in the Rottapharm Agreement referred to below) under the Sale and Purchase Agreement, dated as of July 30, 2014 (the “Rottapharm Agreement”), among Fidim S.r.l., Meda Pharma S.p.A and Meda, the occurrence of which accelerated an unconditional deferred purchase price payment of approximately $308 million (€275 million) relating to Meda’s acquisition of Rottapharm S.p.A. which otherwise would have been payable in January 2017. The amount was paid as of September 30, 2016.
The operating results of Meda have been included in the Company’s Condensed Consolidated Statements of Operations since the acquisition date. The total revenues of Meda for the period from the acquisition date to September 30, 2016, were $331.1 million and net loss, net of tax, was $260.6 million. The net loss, net of tax, includes the effects of the purchase accounting adjustments and acquisition related costs.
Renaissance Topicals Business
On June 15, 2016, the Company completed the acquisition of the non-sterile, topicals-focused business (the “Topicals Business”) of Renaissance Acquisition Holdings, LLC (“Renaissance”) for approximately $1.0 billion in cash at closing, including amounts deposited into escrow for potential contingent payments, subject to customary adjustments. The Topicals Business providesprovided the Company with a complementary portfolio of approximately 25 products, an active pipeline of approximately 25 products, and an established U.S. sales and marketing infrastructure targeting dermatologists. The Topicals Business also providesprovided an integrated manufacturing and development platform. In accordance with U.S. GAAP, the Company

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used the acquisition method of accounting to account for this transaction. Under the acquisition method of accounting, the assets acquired and liabilities assumed in the transaction were recorded at their respective estimated fair values at the acquisition date. The U.S. GAAP purchase price was $972.7 million, which includes estimated contingent consideration of approximately $16 million related to the potential $50 million payment contingent on the achievement of certain 2016 financial targets. The $50 million contingent payment has been paid into escrow. remains in escrow and is classified as restricted cash included in prepaid expenses and other current assets on the Condensed Consolidated Balance Sheets at March 31, 2017 and December 31, 2016.
The preliminary allocation of the $972.7 million purchase price to the assets acquired and liabilities assumed for the Topicals Business is as follows:

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(In millions)  
Current assets (excluding inventories)$68.8
$57.7
Inventories74.2
74.2
Property, plant and equipment54.8
54.8
Identified intangible assets467.0
467.0
In-process research and development275.0
275.0
Goodwill307.3
318.6
Other assets0.9
0.1
Total assets acquired1,248.0
1,247.4
Current liabilities(65.0)(74.2)
Deferred tax liabilities(203.6)(194.6)
Other noncurrent liabilities(6.7)(5.9)
Net assets acquired$972.7
$972.7
The preliminary fair value estimates for the assets acquired and liabilities assumed were based upon preliminary calculations, valuations and assumptions that are subject to change as the Company obtains additional information during the measurement period (up to one year from the acquisition date). The primary areas subject to change relate to the finalization of the working capital adjustmentcomponents and income taxes.
The acquisition of the Topicals Business broadened the Company’s dermatological portfolio. The amount allocated to in-process research and development (“IPR&D”) represents an estimate of the fair value of purchased in-process technology for research projects that, as of the closing date of the acquisition, had not reached technological feasibility and had no alternative future use. The fair value of IPR&D of $275.0 million was based on the excess earnings method, which utilizes forecasts of expected cash inflows (including estimates for ongoing costs) and other contributory charges. A discount rate of 12.5% was utilized to discount net cash inflows to present values. IPR&D is accounted for as an indefinite-lived intangible asset and will be subject to impairment testing until completion or abandonment of the projects. Upon successful completion and launch of each product, the Company will make a determination of the estimated useful life of the individual asset. The acquired IPR&D projects are in various stages of completion and the estimated costs to complete these projects total approximately $65$59 million, which is expected to be incurred through 2018. There are risks and uncertainties associated with the timely and successful completion of the projects included in IPR&D, and no assurances can be given that the underlying assumptions used to estimate the fair value of IPR&D will not change or the timely completion of each project to commercial success will occur.
The identified intangible assets of $467.0 million are comprised of $454.0 million of product rights and licenses that have a weighted average useful life of 14 years and $13.0 million of contract manufacturing agreements that have a weighted average useful life of five years. Significant assumptions utilized in the valuation of identified intangible assets were based on company specific information and projections which are not observable in the market and are thus considered Level 3 measurements as defined by U.S. GAAP.
The goodwill of $307.3$318.6 million arising from the acquisition consisted largely of the value of the employee workforce and the expected value of products to be developed in the future. All of the goodwill was assigned to the GenericsNorth America segment. None of the goodwill recognized in this transaction is currently expected to be deductible for income tax purposes. Acquisition related costs of approximately $3.6 million were incurred during the nine months ended September 30, 2016 related to this transaction, which were recorded as a component of SG&A in the Condensed Consolidated Statements of Operations. The acquisition did not have a material impact on the Company’s results of operations since the acquisition date or on a pro forma basis for the three and nine month periodsperiod ended September 30, 2016 and 2015.
Jai Pharma Limited
On November 20, 2015, the Company completed the acquisition of certain female healthcare businesses from Famy Care Limited (such businesses “Jai Pharma Limited”). Jai Pharma Limited is a specialty women’s healthcare company with global leadership in generic oral contraceptive products, through its wholly owned subsidiary Mylan Laboratories Limited forMarch 31, 2016.

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a cash payment of $750 million plus additional contingent payments of up to $50 million for the filing for approval with, and receipt of approval from, the U.S. Food and Drug Administration of a product under development by Jai Pharma Limited.
In accordance with U.S. GAAP, the Company used the acquisition method of accounting to account for this transaction. Under the acquisition method of accounting, the assets acquired and liabilities assumed in the transaction were recorded at their respective estimated fair values at the acquisition date. The U.S. GAAP purchase price was $711.1 million, which excludes the $50 million paid into escrow at closing that is contingent upon at least one of two former principal shareholders of Jai Pharma Limited continuing to provide consulting services to Jai Pharma Limited for the two year post-closing period, which amount is being treated as compensation expense over the service period. The U.S. GAAP purchase price also excludes $7 million of working capital and other adjustments and includes estimated contingent consideration of approximately $18 million related to the $50 million contingent payment. During the nine months ended September 30, 2016, adjustments were made to the preliminary purchase price allocation recorded at November 20, 2015. The adjustments recorded in respect of goodwill, current liabilities and deferred tax liabilities are reflected in the “measurement period adjustments” column of the table below. As of September 30, 2016, the preliminary allocation of the $711.1 million purchase price to the assets acquired and liabilities assumed for Jai Pharma Limited is as follows:
(In millions)
Preliminary Purchase Price Allocation as of November 20, 2015 (a)
 
Measurement Period Adjustments (b)
 
Preliminary Purchase Price Allocation as of September 30, 2016
 (as adjusted)
Current assets (excluding inventories)$25.7
 $
 $25.7
Inventories4.9
 
 4.9
Property, plant and equipment17.2
 
 17.2
Identified intangible assets437.0
 
 437.0
In-process research and development98.0
 
 98.0
Goodwill317.2
 8.1
 325.3
Other assets0.7
 
 0.7
Total assets acquired900.7
 8.1
 908.8
Current liabilities(9.1) (1.9) (11.0)
Deferred tax liabilities(180.5) (6.2) (186.7)
Net assets acquired$711.1
 $
 $711.1
____________ 
(a)
As previously reported in the Company’s Annual Report on Form 10-K for the year ended December 31, 2015, as amended.
(b)
The measurement period adjustments were recorded in the first quarter of 2016 and are related to the recognition of certain goodwill, current liabilities and adjustments to deferred tax liabilities to reflect facts and circumstances that existed as of the acquisition date.
The goodwill of $325.3 million arising from the acquisition consisted largely of the value of the employee workforce and the expected value of products to be developed in the future. All of the goodwill was assigned to the Generics segment. The preliminary fair value estimates for the assets acquired and liabilities assumed were based upon preliminary calculations, valuations and assumptions that are subject to change as the Company obtains additional information during the measurement period (up to one year from the acquisition date). The primary areas subject to change relate to the finalization of the working capital adjustment and income taxes, which will be finalized in the fourth quarter of 2016. During the three months ended September 30, 2016, the Company received approvals from the relevant Indian regulatory authorities to legally merge its wholly owned subsidiary, Jai Pharma Limited, into Mylan Laboratories Limited. The merger resulted in the recognition of a deferred tax asset of $150 million for the tax deductible goodwill in excess of the book goodwill with a corresponding benefit to income tax provision for the three and nine months ended September 30, 2016. On a pro forma basis, the acquisition did not have a material impact on the Company’s results of operations for the three and nine months ended September 30, 2015.

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EPD Business
On February 27, 2015 (the “EPD Transaction Closing Date”), the Company completed the acquisition (the “EPD Transaction”) of Mylan Inc. and Abbott Laboratories’ non-U.S. developed markets specialty and branded generics business (the “EPD Business”) in an all-stock transaction. Mylan N.V.’s purchase price for the EPD Business, which was on a debt-free basis, was $6.31 billion based on the closing price of Mylan Inc.’s stock as of the EPD Transaction Closing Date, as reported by the NASDAQ.
The operating results of the EPD Business have been included in the Company’s Condensed Consolidated Statements of Operations since February 27, 2015. The total revenues of the acquired EPD Business for the period from the acquisition date to September 30, 2015 were $1.01 billion and the net loss, net of tax, was $68.6 million. The net loss, net of tax, includes the effects of the purchase accounting adjustments and acquisition related costs.
Unaudited Pro Forma Financial Results
The following table presents supplemental unaudited pro forma information for the acquisitionsacquisition of Meda, as if it had occurred on January 1, 2015, and the EPD Business, as if it had occurred on January 1, 2014.2015. The unaudited pro forma results reflect certain adjustments related to past operating performance and acquisition accounting adjustments, such as increased amortization expense based on the fair value of assets acquired, the impact of transaction costs and the related income tax effects. The unaudited pro forma results do not include any anticipated synergies which may be achievable, or have been achieved, subsequent to the closing of the Meda transaction and EPD Transaction.transaction. Accordingly, the unaudited pro forma results are not necessarily indicative of the results that actually would have occurred had the acquisitions been completed on the stated dates above, nor are they indicative of the future operating results of Mylan N.V. and its subsidiaries.
Three Months Ended Nine Months EndedThree Months Ended
September 30, September 30,March 31,
(Unaudited, in millions, except per share amounts)2016 2015 2016 20152016
Total revenues$3,168.6
 $3,506.4
 $9,008.2
 $8,895.0
$2,687.7
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders$(111.4) $381.2
 $132.0
 $405.8
(Loss) earnings per ordinary share attributable to Mylan N.V. ordinary shareholders:       
Net earnings$10.1
Earnings per ordinary share: 
Basic$(0.21) $0.74
 $0.25
 $0.78
$0.02
Diluted$(0.21) $0.71
 $0.25
 $0.75
$0.02
Weighted average ordinary shares outstanding:        
Basic533.9
 516.9
 526.9
 517.0
518.0
Diluted533.9
 540.4
 536.2
 544.0
537.8
Other Transactions
During the second quarter of 2016,On March 29, 2017, the Company entered into an agreementannounced that it had completed its acquisition of the global rights to acquire a marketed pharmaceutical productthe Cold-EEZE® brand cold remedy line from ProPhase Labs, Inc. for an upfront payment of approximately $57.9$50 million which is included in investing activities in the Condensed Consolidated Statements of Cash Flows.cash. The Company accounted for this transaction as an asset acquisition and the asset is amortizing the product rightbeing amortized over a weighted useful life of five15 years.
On January 8, 2016,February 14, 2017, the Company entered into an agreement with Momenta Pharmaceuticals, Inc. (“Momenta”) to develop, manufacture and commercialize up to six of Momenta’s current biosimilar candidates, including Momenta’s biosimilar candidate, ORENCIA® (abatacept). As part of the agreement, Mylan made an up-front cash payment of $45 million to Momenta. Under the terms of the agreement, Momenta is eligible to receive additional contingent milestone payments of up to $200 million. The Company and Momenta will jointly be responsible for producta joint development and will equally sharemarketing agreement for a respiratory product that resulted in approximately $50 million in research and development (“R&D”) expense in the costs and profits related to the products. Under the agreement, Mylan will lead the worldwide commercialization efforts.
On November 2, 2016, the Company and Momenta announced that dosing had begun in a Phase 1 study to compare the pharmacokinetics, safety and immunogenicity of M834, a proposed bisoimilar or ORENCIA® (abatacept), to U.S. and

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European Union sourced ORENCIA® in normal healthy volunteers. Under the agreement, Momenta has achieved the milestone necessary to earn a $25 million payment from the Company which will be paid in the fourthfirst quarter of 2016.
In accordance with ASC 730, Research and Development,the Company is accounting for the contingent milestone payments as non-refundable advance payments for services to be used in future R&D activities, which are required to be capitalized until the related services have been performed. More specifically, as costs are incurred within the scope of the collaboration, the Company will record its share of the costs as R&D expense. In addition to the upfront cash payment, during the three and nine months ended September 30, 2016 the Company incurred approximately $9.0 million and $22.3 million, respectively, of R&D expense related to this collaboration. To the extent the contingent milestone payments made by the Company exceed the liability incurred, a prepaid asset will be reflected on the Company’s Condensed Consolidated Balance Sheet. To the extent the contingent milestone payments made by the Company are less than the expense incurred, the difference between the payment and the expense will be recorded as a liability on the Company’s Condensed Consolidated Balance Sheet.2017.
5.Share-Based Incentive Plan
The Company’s shareholders have approved the 2003 Long-Term Incentive Plan (as amended, the “2003 Plan”). Under the 2003 Plan, 55,300,000 ordinary shares are reserved for issuance to key employees, consultants, independent contractors and non-employee directors of the Company through a variety of incentive awards, including: stock options, stock appreciation rights (“SAR”), restricted ordinary shares and units, performance awards (“PSU”), other stock-based awards and short-term cash awards. Stock option awards are granted atwith an exercise price equal to the fair market value of the ordinary shares underlying the options at the date of the grant, generally become exercisable over periods ranging from three to four years, and generally expire in ten years. UponSince approval of the 2003 Plan, no further grants of stock options have been made under any other previous plans.
The following table summarizes stock option and SAR (“stock awards”) activity:
 
Number of Shares
Under Stock Awards
 
Weighted
Average
Exercise Price
per Share
Outstanding at December 31, 20157,732,499
 $31.85
Granted780,254
 46.15
Exercised(496,440) 23.52
Forfeited(166,571) 51.26
Outstanding at September 30, 20167,849,742
 $33.39
Vested and expected to vest at September 30, 20167,537,727
 $32.78
Exercisable at September 30, 20165,704,835
 $27.71
As of September 30, 2016, stock awards outstanding, stock awards vested and expected to vest and stock awards exercisable had average remaining contractual terms of 6.0 years, 5.9 years and 5.0 years, respectively. Also, at September 30, 2016, stock awards outstanding, stock awards vested and expected to vest and stock awards exercisable had aggregate intrinsic values of $75.9 million, $75.7 million and $75.0 million, respectively.plan.

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The following table summarizes stock option and SAR (together, “stock awards”) activity:
 
Number of Shares
Under Stock Awards
 
Weighted
Average
Exercise Price
per Share
Outstanding at December 31, 20167,699,441
 $33.38
Granted706,995
 45.02
Exercised(242,795) 21.27
Forfeited(161,159) 50.43
Outstanding at March 31, 20178,002,482
 $34.43
Vested and expected to vest at March 31, 20177,723,468
 $33.98
Exercisable at March 31, 20175,976,527
 $30.24
As of March 31, 2017, stock awards outstanding, stock awards vested and expected to vest, and stock awards exercisable had average remaining contractual terms of 5.9 years, 5.8 years and 4.9 years, respectively. Also, at March 31, 2017, stock awards outstanding, stock awards vested and expected to vest and stock awards exercisable had aggregate intrinsic values of $73.5 million, $73.4 million and $73.0 million, respectively.
A summary of the status of the Company’s nonvested restricted stockordinary shares and restricted stock unit awards, including performance restricted stock units and restricted ordinary sharesPSUs (collectively, “restricted stock awards”), as of September 30, 2016March 31, 2017 and the changes during the ninethree months ended September 30, 2016March 31, 2017 are presented below:
Number of
Restricted
Stock Awards
 
Weighted  Average
Grant-Date
Fair Value per  Share
Number of
Restricted
Stock Awards
 
Weighted  Average
Grant-Date
Fair Value per  Share
Nonvested at December 31, 20154,474,436
 $40.70
Nonvested at December 31, 20165,667,830
 $42.46
Granted2,619,679
 45.15
1,255,062
 45.17
Released(1,072,156) 41.95
(483,902) 52.54
Forfeited(326,916) 41.65
(117,259) 49.99
Nonvested at September 30, 20165,695,043
 $42.49
Nonvested at March 31, 20176,321,731
 $42.09
As of September 30, 2016March 31, 2017, the Company had $165.0181.8 million of total unrecognized compensation expense, net of estimated forfeitures, related to all of its stock-based awards, which will be recognized over the remaining weighted average vesting period of 2.42.2 years. The total intrinsic value of stock awards exercised and restricted stock units released during the ninethree months ended September 30, 2016March 31, 2017 and 20152016 was $49.126.1 million and $254.940.1 million, respectively.
6.Pensions and Other Postretirement Benefits
Defined Benefit Plans
The Company sponsors various defined benefit pension plans in several countries. Benefits provided generally depend on length of service, pay grade and remuneration levels. The Company maintains an historic smalltwo fully frozen defined benefit pension planplans in the U.S., and employees in the U.S. and Puerto Rico are generally provided retirement benefits through defined contribution plans. The Company acquired net unfunded pension and other postretirement liabilities of approximately $322.3 million as a result of the Meda transaction.
The Company also sponsors other postretirement benefit plans. There areplans including plans that provide for postretirement supplemental medical coverage. Benefits from these plans are paidprovided to employees and their spouses and dependents who meet various minimum age and service requirements. In addition, there arethe Company sponsors other plans that provide for life insurance benefits and postretirement medical coverage for certain officers and management employees.
Net Periodic Benefit Cost
Components of net periodic benefit cost for the three and nine months ended September 30,March 31, 2017 and 2016 and 2015 were as follows:
 Pension and Other Postretirement Benefits
 Three Months Ended Nine Months Ended
 September 30, September 30,
(In millions)2016 2015 2016 2015
Service cost$4.8
 $2.8
 $12.6
 $8.5
Interest cost2.8
 1.2
 5.7
 3.6
Expected return on plan assets(3.0) (1.4) (7.0) (4.1)
Plan curtailment, settlement and termination
 0.3
 
 0.8
Amortization of prior service costs0.1
 0.1
 0.2
 0.2
Recognized net actuarial losses0.2
 0.3
 0.7
 0.9
Net periodic benefit cost$4.9
 $3.3
 $12.2
 $9.9
The Company is making the minimum mandatory contributions to its U.S. defined benefit pension plans in the 2016 plan year. The Company expects to make total benefit payments of approximately $20.2 million and contributions to pension and other postretirement benefit plans of approximately $17.7 million in 2016.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


7.Balance Sheet Components
Selected balance sheet components consist of the following:
(In millions)September 30,
2016
 December 31,
2015
Inventories:   
Raw materials$825.1
 $592.4
Work in process469.8
 387.0
Finished goods1,392.6
 971.6
 $2,687.5
 $1,951.0
Property, plant and equipment:   
Land and improvements$145.0
 $124.5
Buildings and improvements1,074.9
 950.6
Machinery and equipment2,215.6
 1,928.4
Construction in progress344.8
 290.5
Gross property, plant and equipment3,780.3
 3,294.0
Accumulated depreciation1,496.1
 1,310.1
Property, plant and equipment, net$2,284.2
 $1,983.9
Other current liabilities:   
Legal and professional accruals, including litigation accruals$610.8
 $122.6
Payroll and employee benefit plan accruals429.7
 367.9
Accrued sales allowances824.1
 681.8
Accrued interest114.3
 25.1
Fair value of financial instruments25.2
 19.8
Compulsory acquisition proceeding431.0
 
Other1,210.7
 624.7
 $3,645.8
 $1,841.9

Included in prepaid expenses and other current assets in the Condensed Consolidated Balance Sheets was $156.8 million and $106.6 million of restricted cash at September 30, 2016 and December 31, 2015, respectively. During the nine months ended September 30, 2016, the Company recorded restricted cash of approximately $50 million related to amounts deposited in escrow, for potential contingent consideration payments related to the acquisition of the Topicals Business. An additional $100 million of restricted cash was classified in other long-term assets at December 31, 2015, principally related to amounts deposited in escrow, or restricted amounts, for potential contingent consideration payments related to the acquisition of Agila Specialties Private Limited (“Agila”), which the Company acquired in 2013 from Strides Arcolab Limited (“Strides”). At September 30, 2016, this amount was reclassified to current restricted cash in conjunction with the Strides Settlement, as defined in Note 18 Contingencies.
Included in legal and professional accruals, including litigation accruals at September 30, 2016 is $465 million for a settlement with the U.S. Department of Justice and other government agencies related to the classification of the EpiPen® Auto-Injector and EpiPen Jr® Auto-Injector (collectively, “EpiPen® Auto-Injector”) for purposes of the Medicaid Drug Rebate Program (the “Medicaid Drug Rebate Program Settlement”), as discussed further in Note 18 Contingencies.
At the close of the Meda transaction and at September 30, 2016, the Company recorded a current liability of $431 million related to the purchase of the non-tendered shares of Meda pursuant to the compulsory acquisition proceeding. Included in other current liabilities at September 30, 2016 is approximately $350 million of accrued expenses assumed from Meda.
Contingent consideration included in other current liabilities totaled $128.6 million and $35.0 million at September 30, 2016 and December 31, 2015, respectively. During the nine months ended September 30, 2016, the Company recorded

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


contingent consideration
 Pension and Other Postretirement Benefits
 March 31,
(In millions)2017 2016
Service cost$5.0
 $3.9
Interest cost3.7
 1.5
Expected return on plan assets(3.5) (2.0)
Amortization of prior service costs0.1
 0.1
Recognized net actuarial losses0.2
 0.2
Net periodic benefit cost$5.5
 $3.7
The Company is making the minimum mandatory contributions to its U.S. defined benefit pension plans in the 2017 plan year. The Company expects to make total benefit payments of $16approximately $30.4 million and contributions to pension and other postretirement benefit plans of approximately $30.2 million in 2017.
7.Balance Sheet Components
Selected balance sheet components consist of the following:
Inventories
(In millions)March 31,
2017
 December 31,
2016
Raw materials$833.8
 $783.4
Work in process427.3
 436.0
Finished goods1,286.7
 1,237.0
Inventories$2,547.8
 $2,456.4
Prepaid and other current liabilitiesassets related
(In millions)March 31,
2017
 December 31, 2016
Prepaid expenses$177.0
 $169.1
Restricted cash135.8
 148.1
Available-for-sale securities91.3
 83.7
Fair value of financial instruments88.2
 62.2
Trading securities30.7
 29.6
Other current assets398.9
 263.7
Prepaid expenses and other current assets$921.9
 $756.4
Prepaid expenses consist primarily of prepaid rent, insurance and other individually insignificant items.

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Notes to the acquisition of the Topicals BusinessCondensed Consolidated Financial Statements (Unaudited) - Continued


Property, plant and made $15.5 million of contingent consideration payments. During the third quarter of 2016,equipment, net
(In millions)March 31,
2017
 December 31, 2016
Machinery and equipment$2,245.3
 $2,227.9
Buildings and improvements1,124.8
 1,106.5
Construction in progress330.4
 328.8
Land and improvements147.6
 144.7
Gross property, plant and equipment3,848.1
 3,807.9
Accumulated depreciation1,510.1
 1,485.7
Property, plant and equipment, net$2,338.0
 $2,322.2
Other assets
(In millions)March 31,
2017
 December 31, 2016
Equity method investments, clean energy investments$305.6
 $320.6
Equity method investments, Sagent Agila58.6
 75.8
Other long-term assets176.8
 172.2
Other assets$541.0
 $568.6
Trade accounts payable
(In millions)March 31,
2017
 December 31,
2016
Trade accounts payable$749.6
 $939.5
Other payables391.8
 408.6
Trade accounts payable$1,141.4
 $1,348.1
Other current liabilities
(In millions)March 31,
2017
 December 31, 2016
Accrued sales allowances$616.5
 $809.0
Legal and professional accruals, including litigation accruals723.2
 720.4
Payroll and employee benefit plan accruals326.8
 409.8
Contingent consideration244.8
 256.9
Accrued interest130.7
 41.0
Restructuring77.2
 138.6
Equity method investments, clean energy investments65.3
 64.7
Fair value of financial instruments8.5
 15.3
Compulsory acquisition proceeding
 70.2
Other833.4
 732.6
Other current liabilities$3,026.4
 $3,258.5
On March 31, 2017, the Company recorded approximately $90 millionannounced that Meridian Medical Technologies (“Meridian”), a Pfizer company that manufactures for the EpiPen® Auto-Injector, expanded a voluntary recall of select lots of EpiPen® Auto-Injector and EpiPen Jr® Auto-Injector to include additional contingent considerationlots distributed in the U.S. and other current liabilitiesmarkets in consultation with the U.S. Food and Drug Administration (“FDA”) (the “EpiPen® Auto-Injector Recall”). This recall was conducted as a result of the Strides Settlement, as definedreceipt of two previously disclosed reports outside of the U.S. of the failure to activate the device due to a potential defect in a supplier component. Both reports were related to the single lot that was previously recalled. The expanded voluntary recall was initiated

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


in the U.S. and also extends to additional markets in Europe, Asia, North and South America. The Company is replacing recalled devices at no cost to the consumer. Estimated costs to Mylan related to product recalls are based on a formal campaign soliciting return of the product and are accrued when they are deemed to be probable and can be reasonably estimated. As of March 31, 2017, the Company recorded an accrual with respect to the recall but there can be no assurance that future costs related to the recall will not exceed amounts recorded. In addition, Meridian is contractually obligated to reimburse Mylan for costs related to the EpiPen® Auto-Injector Recall, and the Company has recorded an asset for the recovery of such costs.
In March 2017, the Company completed the compulsory acquisition proceeding and settled the associated liability. The Meda shareholders whose shares were subject to the compulsory acquisition proceeding received cash consideration plus statutory interest for their Meda shares totaling approximately $71.6 million. Refer to Note 184 ContingenciesAcquisitions and Other Transactions. Contingent consideration included in other for additional information.
Other long-term obligations was $522.9 million and $491.4 million at September 30, 2016 and December 31, 2015, respectively.
(In millions)March 31,
2017
 December 31, 2016
Employee benefit liabilities$387.1
 $396.7
Contingent consideration321.2
 307.7
Equity method investments, clean energy investments288.5
 302.3
Tax contingencies240.5
 239.3
Other135.2
 112.6
Other long-term obligations$1,372.5
 $1,358.6
8.Equity Method Investments
The Company has five equity method investments in limited liability companies that own refined coal production plants (the “clean energy investments”), whose activities qualify for income tax credits under Section 45 of the U.S. Internal Revenue Code of 1986, as amended. In addition,
Since December 2013, the Company holdsheld a 50% interest in Sagent Agila LLC (“Sagent Agila”), which is accounted for using the equity method of accounting. Sagent Agila was a joint venture established to allow for the development, manufacturingdevelop, manufacture and distribution ofdistribute certain generic injectable products in the U.S. market.
The carrying valuesIn April 2017, the Company and respective balance sheet accountsSagent Pharmaceuticals Inc. (“Sagent”) finalized an agreement to dissolve the joint venture. Under the terms of the Company’s clean energy investments andagreement, Mylan received Sagent’s interest in the joint venture in exchange for an approved product right. The assets in the joint venture consisted entirely of product rights for commercialized generic injectables. As a result of this transaction, during the three months ended March 31, 2017, the Company recognized a loss of $5.7 million as a component of net losses from equity method investments. Additionally, during the three months ended March 31, 2017, the Company received a dividend payment of $8.4 million from Sagent Agila, which reduced the carrying value of the equity investment. In the second quarter of 2017, the Company will reclassify its investment in Sagent Agila is as follows at September 30, 2016to product rights and December 31, 2015, respectively:
(In millions)September 30, 2016 December 31, 2015
Clean Energy Investments:   
Other assets$337.6
 $379.3
Total liabilities382.0
 419.3
Other current liabilities64.1
 62.3
Other long-term obligations317.9
 357.0
Sagent Agila:   
Other assets$80.0
 $96.2
licenses and amortize the amount over the remaining estimated useful lives of the products.
Summarized financial information, in the aggregate, for the Company’s significant equity method investments on a 100% basis for the three and nine months ended September 30,March 31, 2017 and 2016 and 2015 are as follows:
Three Months Ended Nine Months EndedThree Months Ended
September 30, September 30,March 31,
(In millions)2016 2015 2016 20152017 2016
Total revenues$170.0
 $205.7
 $418.2
 $492.2
$122.9
 $144.0
Gross (loss) profit(3.0) (3.5) (3.8) (4.0)
Gross loss(2.7) (0.3)
Operating and non-operating expense6.3
 6.9
 16.3
 18.7
5.8
 5.7
Net loss$(9.3) $(10.4) $(20.1) $(22.7)$(8.5) $(6.0)
The Company’s net losses from the six equity method investments includes amortization expense related to the excess of the cost basis of the Company’s investment to the underlying assets of each individual investee. For the three months ended September 30,March 31, 2017 and 2016, and 2015, the Company recognized net losses from equity method investments of $29.7$33.2 million and $27.8 million, respectively. For the nine months ended September 30, 2016 and 2015, the Company recognized net losses from equity method investments$30.9

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


million, respectively, which was recognized as a component of other expense, net in the Condensed Consolidated Statements of Operations. The Company recognizes the income tax credits and benefits from the clean energy investments as part of its provision for income taxes.
9.
Earnings per Ordinary Share Attributable to Mylan N.V.
Basic earnings per ordinary share is computed by dividing net earnings attributable to Mylan N.V. ordinary shareholders by the weighted average number of ordinary shares outstanding during the period. Diluted earnings per ordinary share is computed by dividing net earnings attributable to Mylan N.V. ordinary shareholders by the weighted average number of ordinary shares outstanding during the period increased by the number of additional shares that would have been outstanding related to potentially dilutive securities or instruments, if the impact is dilutive.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


On August 5, 2016, in conjunction with the Offer, the Company issued approximately 26.4 million Mylan N.V. ordinary shares to Meda shareholders. The impact of the issuance of these ordinary shares is included in the calculation of basic earnings per share. The weighted average impact for the three and nine months ended September 30, 2016, was 16.1 million and 5.4 million ordinary shares, respectively.
On September 15, 2008, concurrent with the sale of $575 million aggregate principal amount of Cash Convertible Notes due 2015 (the “Cash Convertible Notes”), Mylan Inc. entered into convertible note hedge and warrant transactions with certain counterparties. In connection with the consummation of the EPD Transaction, the terms of the convertible note hedge were adjusted so that the cash settlement value would be based on Mylan N.V. ordinary shares. The terms of the warrant transactions were also adjusted so that, from and after the consummation of the EPD Transaction, the Company could settle the obligations under the warrant transactions by delivering Mylan N.V. ordinary shares. Pursuant to the warrant transactions, and a subsequent amendment in 2011, there were approximately 43.2 million warrants outstanding, with approximately 41.0 million of the warrants that had an exercise price of $30.00. The remaining warrants had an exercise price of $20.00. The warrants met the definition of derivatives under the FASB’s guidance regarding accounting for derivative instruments and hedging activities; however, because these instruments were determined to be indexed to the Company’s own ordinary shares and met the criteria for equity classification under the FASB’s guidance regarding contracts in an entity’s own equity, the warrants were recorded in shareholders’ equity in the Condensed Consolidated Balance Sheets. On April 15, 2016, in connection with the expiration and settlement of the Company’s equity classified warrants, the Company issued approximately 17.0 million Mylan N.V. ordinary shares. The impact of the issuance of these ordinary shares is included in the calculation of basic earnings per share from the date of issuance. For the nine months ended September 30, 2016, 10.4 million ordinary shares is the weighted average impact included in the calculation of basic earnings per ordinary share. The dilutive impact of the warrants, prior to settlement, is included in the calculation of diluted earnings per ordinary share based upon the average market value of the Company’s ordinary shares during the period as compared to the exercise price. For the ninethree months ended September 30,March 31, 2016, 6.616.7 million warrants were included in the calculation of diluted earnings per ordinary share. For the three
Basic and nine months ended September 30, 2015, 20.3 million and 22.1 million warrants, respectively, were included in the calculation of diluted earnings per ordinary share.
Basic and diluted (loss) earnings per ordinary share attributable to Mylan N.V. are calculated as follows:
Three Months Ended Nine Months EndedThree Months Ended
September 30, September 30,March 31,
(In millions, except per share amounts)2016 2015 2016 20152017 2016
Basic (loss) earnings attributable to Mylan N.V. ordinary shareholders (numerator):       
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders$(119.8) $428.6
 $62.5
 $653.0
Basic earnings (numerator):   
Net earnings$66.4
 $13.9
Shares (denominator):          
Weighted average ordinary shares outstanding523.6
 490.5
 505.9
 466.2
534.5
 489.8
Basic (loss) earnings per ordinary share attributable to Mylan N.V. ordinary shareholders$(0.23) $0.87
 $0.12
 $1.40
Basic earnings per ordinary share$0.12
 $0.03
Diluted (loss) earnings attributable to Mylan N.V. ordinary shareholders (numerator):       
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders$(119.8) $428.6
 $62.5
 $653.0
Diluted earnings (numerator):   
Net earnings$66.4
 $13.9
Shares (denominator):          
Weighted average ordinary shares outstanding523.6
 490.5
 505.9
 466.2
534.5
 489.8
Share-based awards and warrants
 23.5
 9.3
 27.0
2.4
 19.8
Total dilutive shares outstanding523.6
 514.0
 515.2
 493.2
536.9
 509.6
Diluted (loss) earnings per ordinary share attributable to Mylan N.V. ordinary shareholders$(0.23) $0.83
 $0.12
 $1.32
Diluted earnings per ordinary share$0.12
 $0.03
Additional stock awards and restricted stock awards were outstanding during the three and nine months ended September 30, 2016March 31, 2017 and 20152016, but were not included in the computation of diluted earnings per ordinary share for each respective period because the effect would be anti-dilutive. Excluded shares at September 30, 2016March 31, 2017 include certain share-based compensation awards and restricted ordinary shares whose performance conditions had not been fully met. Such excluded shares and anti-dilutive awards represented 4.4 million shares and 6.2 million shares for the three months ended March 31, 2017 and 2016, respectively.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


10.Goodwill and Intangible Assets
The changes in the carrying amount of goodwill for the three months endedMarch 31, 2017 are as follows:
(In millions)North America Segment Europe Segment Rest of World Segment Total
Balance at December 31, 2016:       
Goodwill$3,990.4
 $3,859.1
 $1,767.4
 $9,616.9
Accumulated impairment losses(385.0) 
 
 (385.0)
 3,605.4
 3,859.1
 1,767.4
 9,231.9
Reclassifications(1)
(199.0) 373.2
 (174.2) 
Measurement period adjustments
 1.7
 
 1.7
Divestiture
 (1.3) 
 (1.3)
Foreign currency translation6.6
 77.7
 77.5
 161.8
 $3,413.0
 $4,310.4
 $1,670.7
 $9,394.1
Balance at March 31, 2017:       
Goodwill$3,798.0
 $4,310.4
 $1,670.7
 $9,779.1
Accumulated impairment losses(385.0) 
 
 (385.0)
 $3,413.0
 $4,310.4
 $1,670.7
 $9,394.1
____________
(1)
The reclassifications in the current quarter relate to the allocation of goodwill for the Meda acquisition.
Intangible assets consist of the following components at March 31, 2017 and December 31, 2016:
(In millions)
Weighted
Average Life
(Years)
 
Original
Cost
 
Accumulated
Amortization
 
Net Book
Value
March 31, 2017       
Amortized intangible assets:       
Product rights and licenses15 $17,300.9
 $3,986.2
 $13,314.7
Patents and technologies20 116.6
 109.6
 7.0
Other (1)
6 468.8
 354.7
 114.1
   17,886.3
 4,450.5
 13,435.8
In-process research and development  934.2
 
 934.2
   $18,820.5
 $4,450.5
 $14,370.0
December 31, 2016       
Amortized intangible assets:       
Product rights and licenses15 $16,968.4
 $3,585.7
 $13,382.7
Patents and technologies20 116.6
 108.5
 8.1
Other (1)
6 465.9
 330.0
 135.9
   17,550.9
 4,024.2
 13,526.7
In-process research and development  921.1
 
 921.1
   $18,472.0
 $4,024.2
 $14,447.8
____________
(1)
Other intangible assets consist principally of customer lists, contractual rights and other contracts.
In December 2011, the Company completed the acquisition of the exclusive worldwide rights to develop, manufacture and commercialize a generic equivalent to GlaxoSmithKline’s Advair® Diskus and Seretide® Diskus incorporating Pfizer

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


sharesInc.’s proprietary dry powder inhaler delivery platform (the “respiratory delivery platform”). The Company accounted for this transaction as a purchase of a business and anti-dilutive awards represented 13.9 million shares and 7.3 million sharesutilized the acquisition method of accounting. In conjunction with the Company’s Generic Drug User Fee Agreement goal date, on March 28, 2017, the Company received a complete response letter from the FDA regarding its Abbreviated New Drug Application for the threerespiratory delivery platform. As of March 31, 2017, the Company has an IPR&D asset of $347.2 million and nine months ended September 30, 2016, respectively,related contingent consideration liability of $436.1 million. The Company performed an analysis and 3.9 million sharesvaluation of the IPR&D asset and the fair value of the related contingent consideration liability through the use of a discounted cash flow model. The model contained certain key assumptions including: the expected product launch date, the number of competitors, the timing of competition and a discount factor based on an industry specific weighted average cost of capital. Based on the analysis performed, the Company determined that the IPR&D asset was not impaired at March 31, 2017. Additionally, no significant fair value adjustment was required for the threecontingent consideration. However, resolution of the matters with the FDA, market conditions and nine months ended September 30, 2015.
10.Goodwill and Intangible Assets
Theother factors may result in significant changes in the carrying amount of goodwill for the nine months endedSeptember 30, 2016 are as follows:
(In millions)
Generics
Segment
 
Specialty
Segment
 Total
Balance at December 31, 2015:     
Goodwill$5,031.0
 $734.1
 $5,765.1
Accumulated impairment losses
 (385.0) (385.0)
 5,031.0
 349.1
 5,380.1
Acquisitions (1)
3,984.9
 
 3,984.9
Measurement period adjustments8.1
 
 8.1
Foreign currency translation260.0
 
 260.0
 $9,284.0
 $349.1
 $9,633.1
Balance at September 30, 2016:     
Goodwill$9,284.0
 $734.1
 $10,018.1
Accumulated impairment losses
 (385.0) (385.0)
 $9,284.0
 $349.1
 $9,633.1
____________
(1)
Includes goodwill related to the acquisition of Meda and the Topicals Business totaling $3.68 billion and $307.3 million, respectively.
Intangible assets consist of the following components at September 30, 2016projections and December 31, 2015:
(In millions)
Weighted
Average Life
(Years)
 
Original
Cost
 
Accumulated
Amortization
 
Net Book
Value
September 30, 2016       
Amortized intangible assets:       
Product rights and licenses15 $17,867.4
 $3,434.0
 $14,433.4
Patents and technologies20 116.6
 107.3
 9.3
Other (1)
6 492.5
 311.4
 181.1
   18,476.5
 3,852.7
 14,623.8
In-process research and development  989.6
 
 989.6
   $19,466.1
 $3,852.7
 $15,613.4
December 31, 2015       
Amortized intangible assets:       
Product rights and licenses11 $8,848.6
 $2,652.7
 $6,195.9
Patents and technologies20 116.6
 103.8
 12.8
Other (1)
6 465.3
 189.8
 275.5
   9,430.5
 2,946.3
 6,484.2
In-process research and development  737.7
 
 737.7
   $10,168.2
 $2,946.3
 $7,221.9
____________
(1)
Other intangible assets consist principally of customer lists, contractual rights and other contracts.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


During the nine months ended September 30, 2016, the Company acquired product rights and licenses from Meda and the Topicals Business totaling approximately $8.06 billion and $454.0 million, respectively. Also,assumptions utilized in the perioddiscounted cash flow model, which could lead to material adjustments to the Company acquired IPR&D totaling approximately $275.0 million from the acquisition of the Topicals Business, and reclassified approximately $20.7 million of previously acquired IPR&D to product rights and licenses.recorded amounts.
Amortization expense, which is classified primarily within cost of sales in the Condensed Consolidated Statements of Operations for the three and nine months ended September 30,March 31, 2017 and 2016 and 2015 totaled:
Three Months Ended Nine Months EndedThree Months Ended
September 30, September 30,March 31,
(In millions)2016 2015 2016 20152017 2016
Amortization expense$364.3
 $214.3
 $852.9
 $559.8
Intangible asset amortization expense$342.4
 $242.3
Inclusive of the impact from the acquisitions of Meda and the Topicals Business,Intangible asset amortization expense over the remainder of 20162017 and for the years ended December 31, 20172018 through 20202021 is estimated to be as follows:
(In millions)  
2016$362
20171,307
$942
20181,254
1,220
20191,161
1,130
20201,041
1,010
2021936
11.Financial Instruments and Risk Management
The Company is exposed to certain financial risks relating to its ongoing business operations. The primary financial risks that are managed by using derivative instruments are foreign currency risk and interest rate risk.
Foreign Currency Risk Management
In order to manage foreign currency risk, the Company enters into foreign exchange forward contracts to mitigate risk associated with changes in spot exchange rates of mainly non-functional currency denominated assets or liabilities. The foreign exchange forward contracts are measured at fair value and reported as current assets or current liabilities on the Condensed Consolidated Balance Sheets. Any gains or losses on the foreign exchange forward contracts are recognized in earnings in the period incurred in the Condensed Consolidated Statements of Operations.
In order to economically hedge the foreign currency exposure associated with the expected payment of the Swedish krona-denominated cash portion of the purchase price of the Offer, the Company entered into a series of non-designated foreign exchange forward and option contracts with a total notional amount of 45.2kr billion. During the three and nine months ended September 30, 2016, the Company recognized losses of $44.4 million and $128.6 million for the changes in fair value related to these contracts which is included in other expense, net in the Condensed Consolidated Statements of Operations. These contracts settled during the three months ended September 30, 2016.
The Company has also entered into forward contracts to hedge forecasted foreign currency denominated sales from certain international subsidiaries. These contracts are designated as cash flow hedges to manage foreign currency transaction risk and are measured at fair value and reported as current assets or current liabilities on the Condensed Consolidated Balance Sheets. Any changes in fair value are included in earnings or deferred through accumulated other comprehensive earnings (“AOCE”), depending on the nature and effectiveness of the offset. Any ineffectiveness in a cash flow hedging relationship is recognized immediately in earnings in the Condensed Consolidated Statements of Operations.
FollowingIn the acquisitionfirst quarter of Meda,2017, the Company designated certain Euro borrowings as a hedge of its investment in certain Euro-functional currency subsidiaries in order to manage foreign currency translation risk. The notional amount of the net investment hedges was €288 million€1.4 billion and consists primarily of Euro denominated debt which has a maturity date in August 2017. Borrowings designated as net investment hedges are marked to market using the current spot exchange rate as€604 million of the end€1.0 billion aggregate principal amount of 2.250% Senior Notes due 2024 (the “2024 Euro Notes”) and €750 million aggregate principal amount of 3.125% Senior Notes due 2028

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


(the “2028 Euro Notes”). Borrowings designated as net investment hedges are marked to market using the current spot exchange rate as of the end of the period, with gains and losses included in the foreign currency translation component of AOCE until the sale or substantial liquidation of the underlying net investments. The Company recorded no ineffectiveness from its net investment hedges for the three or nine months ended September 30, 2016.March 31, 2017. In addition, the Company manages the related foreign exchange risk of the €500 million aggregate principal amount of floating rate Senior Notes due 2018 (the “Floating Rate Euro Notes”), €750 million aggregate principal amount of 1.250% Euro Senior Notes due 2020 (the “2020 Euro Notes”) and the remaining portion of the 2024 Euro Notes through certain Euro denominated financial assets.
Interest Rate Risk Management
The Company enters into interest rate swaps in order to manage interest rate risk associated with the Company’s fixed-rate and floating-rate debt. These derivative instruments are measured at fair value and reported as current assets or current liabilities in the Condensed Consolidated Balance Sheets.
Cash Flow Hedging Relationships
The Company’s interest rate swaps designated as cash flow hedges fix the interest rate on a portion of the Company’s variable-rate debt or hedge part of the Company’s interest rate exposure associated with variability in future cash flows attributable to changes in interest rates. Any changes in fair value are included in earnings or deferred through AOCE, depending on the nature and effectiveness of the offset. Any ineffectiveness in a cash flow hedging relationship is recognized immediately in earnings in the Condensed Consolidated Statements of Operations.
Following the acquisition of Meda, the Company designated certain interest rate swaps with a notional amount of €750 million as cash flow hedges. The maturity date of these swaps is June 2017.
In September 2015, the Company entered into a series of forward starting swaps to hedge against changes in interest rates related to future debt issuances. These swaps were designated as cash flow hedges of expected future issuances of long-term bonds. The Company executed $500 million of notional value swaps with an effective date of June 2016 and an additional $500 million of notional value swaps with an effective date of November 2016. Both sets of swaps had a maturity of 10 years. As discussed further in Note 12Debt, during the second quarter of 2016, the Company issued $2.25 billion in an aggregate principal amount of 3.950% Senior Notes due 2026 and the Company terminated these swaps. As a result of this termination, the Company recorded losses of $64.9 million in AOCE, which are being amortized over the life of the 3.950% Senior Notes due 2026. In addition, during the second quarter of 2016, approximately $2.1 million of hedge ineffectiveness related to these forward starting swaps was recorded in interest expense on the Condensed Consolidated Statements of Operations.
Fair Value Hedging Relationships
The Company’s interest rate swaps designated as fair value hedges convert the fixed rate on a portion of the Company’s fixed-rate senior notes to a variable rate. Any changes in the fair value of these derivative instruments, as well as the offsetting change in fair value of the portion of the fixed-rate debt being hedged, is included in interest expense.
The Company regularly reviews the creditworthiness of its financial counterparties and does not expect to incur a significant loss from the failure of any counterparties to perform under any agreements. The Company is not subject to any obligations to post collateral under derivative instrument contracts. Certain derivative instrument contracts entered into by the Company are governed by master agreements, which contain credit-risk-related contingent features that would allow the counterparties to terminate the contracts early and request immediate payment should the Company trigger an event of default on other specified borrowings. The Company records all derivative instruments on a gross basis in the Condensed Consolidated Balance Sheets. Accordingly, there are no offsetting amounts that net assets against liabilities.
The Effect of Derivative Instruments on the Condensed Consolidated Balance Sheets
Fair Values of Derivative Instruments
Derivatives Designated as Hedging Instruments
Asset DerivativesAsset Derivatives
September 30, 2016 December 31, 2015March 31, 2017 December 31, 2016
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair ValueBalance Sheet Location Fair Value Balance Sheet Location Fair Value
Interest rate swapsPrepaid expenses and other current assets $66.4
 Prepaid expenses and other current assets $36.3
Prepaid expenses and other current assets $23.9
 Prepaid expenses and other current assets $26.2
Foreign currency forward contractsPrepaid expenses and other current assets 27.2
 Prepaid expenses and other current assets 8.4
Prepaid expenses and other current assets 47.5
 Prepaid expenses and other current assets 21.9
Total $93.6
 $44.7
 $71.4
 $48.1

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 Liability Derivatives
 September 30, 2016 December 31, 2015
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair Value
Interest rate swapsOther current liabilities $1.7
 Other current liabilities $10.5
Total  $1.7
   $10.5

The Effect of Derivative Instruments on the Condensed Consolidated Balance Sheets
Fair Values of Derivative Instruments
Derivatives Not Designated as Hedging Instruments
 Asset Derivatives
 September 30, 2016 December 31, 2015
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair Value
Foreign currency forward contractsPrepaid expenses and other current assets $7.2
 Prepaid expenses and other current assets $20.0
Total  $7.2
   $20.0
 Liability Derivatives
 September 30, 2016 December 31, 2015
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair Value
Foreign currency forward contractsOther current liabilities $23.5
 Other current liabilities $9.3
Total  $23.5
   $9.3
The Effect of Derivative Instruments on theCondensed Consolidated Statements of Operations
Derivatives in Fair Value Hedging Relationships
 
Location of (Loss) Gain
Recognized in Earnings
on Derivatives
 
Amount of (Loss) Gain
Recognized in Earnings on
Derivatives
(In millions) Three Months Ended Nine Months Ended
 September 30, September 30,
 2016 2015 2016 2015
Interest rate swapsInterest expense $(9.7) $29.5
 $30.2
 $34.1
Total  $(9.7) $29.5
 $30.2
 $34.1
 
Location of Gain (Loss)
Recognized in Earnings
on Hedged Items
 
Amount of Gain (Loss)
Recognized in Earnings on
Hedged Items
(In millions) Three Months Ended Nine Months Ended
 September 30, September 30,
 2016 2015 2016 2015
2023 Senior Notes (3.125% coupon)Interest expense $9.7
 $(25.0) $(30.2) $(20.4)
Total  $9.7
 $(25.0) $(30.2) $(20.4)


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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


The Effect of Derivative Instruments on the Condensed Consolidated Statements of Comprehensive EarningsBalance Sheets
Derivatives in Cash Flow Hedging Relationships
  Amount of Gain (Loss)
Recognized in AOCE
(Net of Tax) on Derivative
(Effective Portion)
  Three Months Ended Nine Months Ended
  September 30, September 30,
(In millions) 2016 2015 2016 2015
Foreign currency forward contracts $2.9
 $(21.3) $(16.3) $(36.5)
Interest rate swaps (0.9) (40.3) (38.0) (37.0)
Total $2.0
 $(61.6) $(54.3) $(73.5)
The EffectFair Values of Derivative Instruments on the Condensed Consolidated Statements of Comprehensive Earnings
Derivatives in Net Investment Hedging Relationships
  Amount of Loss Recognized in AOCE
(Net of Tax) on Derivative
(Effective Portion)
  Three Months Ended Nine Months Ended
  September 30, September 30,
(In millions) 2016 2015 2016 2015
Foreign currency borrowings and forward contracts $(8.1) $
 $(8.1) $
Total $(8.1) $
 $(8.1) $

The Effect of Derivative Instruments on the Condensed Consolidated Statements of Operations
Derivatives in Cash Flow Hedging Relationships
 
Location of Loss Reclassified
from AOCE into Earnings
(Effective Portion)
 
Amount of Loss
Reclassified from AOCE
into Earnings
 (Effective Portion)
  Three Months Ended Nine Months Ended
  September 30, September 30,
(In millions) 2016 2015 2016 2015
Foreign currency forward contractsNet sales $(10.7) $(8.1) $(34.2) $(30.4)
Interest rate swapsInterest expense (2.3) (0.2) (6.6) (0.5)
Total  $(13.0) $(8.3) $(40.8) $(30.9)
 
Location of Gain
Excluded from the
Assessment of
Hedge Effectiveness
 
Amount of Gain
 Excluded from the
Assessment of Hedge Effectiveness
  Three Months Ended Nine Months Ended
  September 30, September 30,
(In millions) 2016 2015 2016 2015
Foreign currency forward contractsOther expense, net $8.9
 $11.7
 $26.0
 $35.1
Total  $8.9
 $11.7
 $26.0
 $35.1
At September 30, 2016, the Company expects that approximately $27.8 million of pre-tax net losses on cash flow hedges will be reclassified from AOCE into earnings during the next twelve months.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


The Effect of Derivative Instruments on theCondensed Consolidated Statements of Operations
Derivatives Not Designated as Hedging Instruments
 
Location of (Loss) Gain Recognized
 in Earnings on Derivatives
 
Amount of (Loss) Gain
Recognized in
Earnings on Derivatives
  Three Months Ended Nine Months Ended
  September 30, September 30,
(In millions) 2016 2015 2016 2015
Foreign currency option and forward contractsOther expense, net $(36.8) $22.2
 $(98.3) $29.8
Cash conversion feature of Cash Convertible NotesOther expense, net 
 1,689.3
 
 1,853.5
Purchased cash convertible note hedgeOther expense, net 
 (1,689.3) 
 (1,853.5)
Total  $(36.8) $22.2
 $(98.3) $29.8
 Asset Derivatives
 March 31, 2017 December 31, 2016
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair Value
Foreign currency forward contractsPrepaid expenses and other current assets $16.9
 Prepaid expenses and other current assets $14.0
Total  $16.9
   $14.0
 Liability Derivatives
 March 31, 2017 December 31, 2016
(In millions)Balance Sheet Location Fair Value Balance Sheet Location Fair Value
Foreign currency forward contractsOther current liabilities $8.5
 Other current liabilities $15.3
Total  $8.5
   $15.3
The Effect of Derivative Instruments on theCondensed Consolidated Statements of Operations
Derivatives in Fair Value Hedging Relationships
 
Location of (Loss) Gain
Recognized in Earnings
on Derivatives
 
Amount of (Loss) Gain
Recognized in Earnings on
Derivatives
(In millions) Three Months Ended
 March 31,
 2017 2016
Interest rate swapsInterest expense $(2.4) $29.6
Total  $(2.4) $29.6
 
Location of Gain (Loss)
Recognized in Earnings
on Hedged Items
 
Amount of Gain (Loss)
Recognized in Earnings on
Hedged Items
(In millions) Three Months Ended
 March 31,
 2017 2016
2023 Senior Notes (3.125% coupon)Interest expense $2.4
 $(29.6)
Total  $2.4
 $(29.6)
The Effect of Derivative Instruments on the Condensed Consolidated Statements of Comprehensive Earnings
Derivatives in Cash Flow Hedging Relationships
  Amount of Gain (Loss)
Recognized in AOCE
(Net of Tax) on Derivative
(Effective Portion)
  Three Months Ended
  March 31,
(In millions) 2017 2016
Foreign currency forward contracts $14.1
 $(4.4)
Interest rate swaps 0.7
 (35.9)
Total $14.8
 $(40.3)

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


The Effect of Derivative Instruments on the Condensed Consolidated Statements of Comprehensive Earnings
Derivatives in Net Investment Hedging Relationships
  Amount of Loss Recognized in AOCE
(Net of Tax) on Derivative
(Effective Portion)
  Three Months Ended
  March 31,
(In millions) 2017 2016
Foreign currency borrowings and forward contracts $(9.9) $
Total $(9.9) $
The Effect of Derivative Instruments on the Condensed Consolidated Statements of Operations
Derivatives in Cash Flow Hedging Relationships
 
Location of Loss Reclassified
from AOCE into Earnings
(Effective Portion)
 
Amount of (Loss) Gain
Reclassified from AOCE
into Earnings
 (Effective Portion)
  Three Months Ended
  March 31,
(In millions) 2017 2016
Foreign currency forward contractsNet sales $(5.2) $(10.6)
Interest rate swapsInterest expense (1.8) 0.9
Total  $(7.0) $(9.7)
 
Location of (Loss) Gain
Excluded from the
Assessment of
Hedge Effectiveness
 
Amount of (Loss) Gain
 Excluded from the
Assessment of Hedge Effectiveness
  Three Months Ended
  March 31,
(In millions) 2017 2016
Foreign currency forward contractsOther expense, net $(0.8) $7.3
Total  $(0.8) $7.3
At March 31, 2017, the Company expects that approximately $1 million of pre-tax net losses on cash flow hedges will be reclassified from AOCE into earnings during the next twelve months.
The Effect of Derivative Instruments on theCondensed Consolidated Statements of Operations
Derivatives Not Designated as Hedging Instruments
 
Location of Loss Recognized
 in Earnings on Derivatives
 
Amount of Loss
Recognized in
Earnings on Derivatives
  Three Months Ended
  March 31,
(In millions) 2017 2016
Foreign currency option and forward contractsOther expense, net $(0.3) $(15.0)
Total  $(0.3) $(15.0)
Fair Value Measurement
Fair value is based on the price that would be received from the sale of an identical asset or paid to transfer an identical liability in an orderly transaction between market participants at the measurement date. In order to increase consistency and

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


comparability in fair value measurements, a fair value hierarchy has been established that prioritizes observable and unobservable inputs used to measure fair value into three broad levels, which are described below:
Level 1: Quoted prices (unadjusted) in active markets that are accessible at the measurement date for identical assets or liabilities. The fair value hierarchy gives the highest priority to Level 1 inputs.
Level 2: Observable market-based inputs other than quoted prices in active markets for identical assets or liabilities.
Level 3: Unobservable inputs are used when little or no market data is available. The fair value hierarchy gives the lowest priority to Level 3 inputs.
In determining fair value, the Company utilizes valuation techniques that maximize the use of observable inputs and minimize the use of unobservable inputs to the extent possible, as well as considers counterparty credit risk in its assessment of fair value.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


Financial assets and liabilities carried at fair value are classified in the tables below in one of the three categories described above:
September 30, 2016March 31, 2017
(In millions)Level 1 Level 2 Level 3 TotalLevel 1 Level 2 Level 3 Total
Recurring fair value measurements              
Financial Assets              
Cash equivalents:              
Money market funds$859.9
 $
 $
 $859.9
$275.8
 $
 $
 $275.8
Total cash equivalents859.9
 
 
 859.9
275.8
 
 
 275.8
Trading securities:              
Equity securities — exchange traded funds28.7
 
 
 28.7
30.7
 
 
 30.7
Total trading securities28.7
 
 
 28.7
30.7
 
 
 30.7
Available-for-sale fixed income investments:              
Corporate bonds
 18.3
 
 18.3
U.S. Treasuries
 6.5
 
 6.5

 6.0
 
 6.0
Corporate bonds
 17.6
 
 17.6
Agency mortgage-backed securities
 4.5
 
 4.5

 3.8
 
 3.8
Asset backed securities
 1.5
 
 1.5

 1.6
 
 1.6
Other
 3.9
 
 3.9

 2.2
 
 2.2
Total available-for-sale fixed income investments
 34.0
 
 34.0

 31.9
 
 31.9
Available-for-sale equity securities:              
Marketable securities57.6
 
 
 57.6
59.4
 
 
 59.4
Total available-for-sale equity securities57.6
 
 
 57.6
59.4
 
 
 59.4
Foreign exchange derivative assets
 34.4



34.4

 64.4



64.4
Interest rate swap derivative assets
 66.4
 
 66.4

 23.9
 
 23.9
Total assets at recurring fair value measurement$946.2

$134.8

$

$1,081.0
$365.9

$120.2

$

$486.1
Financial Liabilities              
Foreign exchange derivative liabilities$
 $23.5
 $
 $23.5
$
 $8.5
 $
 $8.5
Interest rate swap derivative liabilities
 1.7



1.7
Contingent consideration
 
 651.5
 651.5

 
 566.0
 566.0
Total liabilities at recurring fair value measurement$
 $25.2
 $651.5
 $676.7
$
 $8.5
 $566.0
 $574.5


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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


December 31, 2015December 31, 2016
(In millions)Level 1 Level 2 Level 3 TotalLevel 1 Level 2 Level 3 Total
Recurring fair value measurements              
Financial Assets              
Cash equivalents:              
Money market funds$923.3
 $
 $
 $923.3
$433.7
 $
 $
 $433.7
Total cash equivalents923.3
 
 
 923.3
433.7
 
 
 433.7
Trading securities:              
Equity securities — exchange traded funds22.8
 
 
 22.8
29.6
 
 
 29.6
Total trading securities22.8
 
 
 22.8
29.6
 
 
 29.6
Available-for-sale fixed income investments:              
Corporate bonds
 17.5
 
 17.5
U.S. Treasuries
 4.7
 
 4.7

 6.0
 
 6.0
Corporate bonds
 15.7
 
 15.7
Agency mortgage-backed securities
 3.9
 
 3.9

 4.0
 
 4.0
Asset backed securities
 2.3
 
 2.3

 1.6
 
 1.6
Other
 1.4
 
 1.4

 2.3
 
 2.3
Total available-for-sale fixed income investments
 28.0
 
 28.0

 31.4
 
 31.4
Available-for-sale equity securities:              
Marketable securities26.0
 
 
 26.0
52.3
 
 
 52.3
Total available-for-sale equity securities26.0
 
 
 26.0
52.3
 
 
 52.3
Foreign exchange derivative assets
 28.4
 
 28.4

 35.9
 
 35.9
Interest rate swap derivative assets
 36.3
 
 36.3

 26.2
 
 26.2
Total assets at recurring fair value measurement$972.1
 $92.7
 $
 $1,064.8
$515.6
 $93.5
 $
 $609.1
Financial Liabilities              
Foreign exchange derivative liabilities$
 $9.3
 $
 $9.3
$
 $15.3
 $
 $15.3
Interest rate swap derivative liabilities
 10.5
 
 10.5
Contingent consideration
 
 526.4
 526.4

 
 564.6
 564.6
Total liabilities at recurring fair value measurement$
 $19.8
 $526.4
 $546.2
$
 $15.3
 $564.6
 $579.9
For financial assets and liabilities that utilize Level 2 inputs, the Company utilizes both direct and indirect observable price quotes, including the LIBOR yield curve, foreign exchange forward prices and bank price quotes. Below is a summary of valuation techniques for Level 1 and Level 2 financial assets and liabilities:
Cash equivalents — valued at observable net asset value prices.
Trading securities — valued at the active quoted market price from broker or dealer quotations or transparent pricing sources at the reporting date.
Available-for-sale fixed income investments — valued at the quoted market price from broker or dealer quotations or transparent pricing sources at the reporting date.
Available-for-sale equity securities — valued using quoted stock prices from public exchanges at the reporting date and translated to the U.S. Dollar at prevailing spot exchange rates, as applicable.date.
Interest rate swap derivative assets and liabilities — valued using the LIBOR/EURIBOR yield curves at the reporting date. Counterparties to these contracts are highly rated financial institutions.
Foreign exchange derivative assets and liabilities — valued using quoted forward foreign exchange prices and spot rates at the reporting date. Counterparties to these contracts are highly rated financial institutions.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


Contingent Consideration
The fair value measurement of contingent consideration is determined using Level 3 inputs. The Company’s contingent consideration represents a component of the total purchase consideration for the respiratory delivery platform, the acquisition of Agila Specialties (“Agila”), the acquisition of Jaicertain female healthcare businesses from Famy Care Limited (such businesses “Jai Pharma Limited,Limited”), the acquisition of the Topicals Business and certain other acquisitions. The measurement is calculated using unobservable inputs based on the Company’s own assumptions. For the respiratory delivery platform, Jai Pharma Limited, the Topicals Business and certain other acquisitions, significant unobservable inputs in the valuation include the probability and timing of future development and commercial milestones and future profit sharing payments. A discounted cash flow method was used to valueWhen valuing the contingent consideration at September 30, 2016related to the respiratory delivery platform and December 31, 2015, which was calculated asJai Pharma Limited, the present value of the estimated future net cash flowsobligations are derived from a probability assessment based on expectations of when certain milestones or profit share payments occur which are discounted using a market rate of return. DiscountAt March 31, 2017 and December 31, 2016, discount rates ranging from 1.4%0.9% to 9.8%10.0% were utilized in the valuations. For the contingent consideration related to the acquisition of Agila and the acquisition of the Topicals Business, significant unobservable inputs in the valuation include the probability of future payments to the seller of amounts withheld at the closing date. Significant changes in unobservable inputs could result in material changes to the contingent consideration liability. During
A rollforward of the three and nine months endedSeptember 30, 2016, accretion of $10.4 million and $30.7 million, respectively, was recorded in interest expenseactivity in the Condensed Consolidated StatementsCompany’s fair value of Operations. During the three and nine months ended September 30, 2015, accretion of $9.7 million and $28.5 million, respectively, was recorded in interest expensecontingent consideration from December 31, 2016 to March 31, 2017 is as follows:
(In millions)
Current Portion (1)
 
Long-Term Portion (2)
 Total Contingent Consideration
Balance at December 31, 2016$256.9
 $307.7
 $564.6
Payments(16.1) (0.2) (16.3)
Accretion
 7.8
 7.8
Fair value loss(3)
4.0
 5.9
 9.9
Balance at March 31, 2017$244.8
 $321.2
 $566.0
____________
(1)
Included in other current liabilities on the Condensed Consolidated Balance Sheets.
(2)
Included in other long-term obligations on the Condensed Consolidated Balance Sheets.
(3)
Included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations.
2017 Changes to Contingent Consideration: During the three months ended March 31, 2017, the Company recorded a fair value loss of $9.9 million related to Jai Pharma Limited contingent consideration. In addition, the Company made payments of approximately $12.5 million related to the settlement reached with Strides Arcolab Limited in November 2016.
Although the Company has not elected the fair value option for other financial assets and liabilities, any future transacted financial asset or liability will be evaluated for the fair value election.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


12.Debt
Long-Term Debt
A summary of long-term debt is as follows:
(In millions)Coupon September 30,
2016
 December 31,
2015
Current portion of long-term debt:     
2016 Senior Notes (a) *
1.800% $
 $500.1
2016 Senior Notes (b) *
1.350% 500.0
 499.9
2015 Term Loans (c)
  1,600.0
 
Meda Bank Loans (d)
  1,942.6
 
Meda Bank Loans (e)
  233.3
 
Other  4.4
 1.6
Deferred financing fees  (1.5) (2.9)
Current portion of long-term debt  $4,278.8
 $998.7
      
Non-current portion of long-term debt:     
2015 Term Loans (c)
  $
 $1,600.0
2014 Term Loan (f)
  800.0
 800.0
Meda Medium Term Notes (g)
  157.5
 
2018 Senior Notes (h) *
2.600% 649.5
 649.3
2018 Senior Notes (h) **
3.000% 499.5
 499.4
2019 Senior Notes (i) **
2.500% 999.0
 
2019 Senior Notes (j) *
2.550% 499.4
 499.2
2020 Senior Notes (k) **
3.750% 499.9
 499.8
2021 Senior Notes (l) **
3.150% 2,247.5
 
2023 Senior Notes (j) *
3.125% 815.4
 785.2
2023 Senior Notes (m) *
4.200% 498.5
 498.4
2026 Senior Notes (n) **
3.950% 2,233.1
 
2043 Senior Notes (o) *
5.400% 497.0
 497.0
2046 Senior Notes (p) **
5.250% 999.8
 
Other  7.8
 2.7
Deferred financing fees  (75.3) (35.4)
Total long-term debt  $11,328.6
 $6,295.6
(In millions)Coupon March 31,
2017
 December 31,
2016
Current portion of long-term debt:     
Meda Bank Loans (a)
  $222.9
 $219.6
Other  4.3
 3.7
Current portion of long-term debt  $227.2
 $223.3
      
Non-current portion of long-term debt:     
2016 Term Loans (b) **
  $1,050.0
 $1,600.0
Meda Medium Term Notes (c)
  148.6
 146.4
2018 Euro Senior Notes (d) **
  532.8
 526.0
2018 Senior Notes (e) *
2.600% 649.6
 649.6
2018 Senior Notes (e) **
3.000% 499.6
 499.6
2019 Senior Notes (f) **
2.500% 999.2
 999.1
2019 Senior Notes (g) *
2.550% 499.5
 499.5
2020 Euro Senior Notes (h) **
1.250% 796.0
 785.7
2020 Senior Notes (i) **
3.750% 499.9
 499.9
2021 Senior Notes (j) **
3.150% 2,247.8
 2,247.7
2023 Senior Notes (g) *
3.125% 772.9
 775.3
2023 Senior Notes (k) *
4.200% 498.6
 498.6
2024 Euro Senior Notes (l)**
2.250% 1,062.8
 1,049.2
2026 Senior Notes (m) **
3.950% 2,233.9
 2,233.5
2028 Euro Senior Notes (n) **
3.125% 791.3
 781.1
2043 Senior Notes (o) *
5.400% 497.1
 497.0
2046 Senior Notes (p) **
5.250% 999.8
 999.8
Other  7.1
 7.1
Deferred financing fees  (85.7) (92.2)
Long-term debt  $14,700.8
 $15,202.9
____________
(a) 
Instrument was due on June 24, 2016, and the Company paid the principal amountRepresents a bank loan of $500.0 million and final interest payment of $4.5 million at that time using available cash on hand.
(b)
Instrument is callable by the Company at any time at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.125% plus,2.0kr billion with AB Svensk Exportkredit (publ), as lender (“Svensk Exportkredit”), which matures in each case, accrued and unpaid interest. Instrument is due on November 29, 2016 and accordingly is included in current portion of long-term debt and other long-term obligations in the Condensed Consolidated Balance Sheets at September 30, 2016.
(c)
The 2015 Term Loans mature on July 15, 2017, subject to extension to December 19, 2017. Accordingly, the 2015 Term Loans are included in current portion of long-term debt and other long-term obligations in the Condensed Consolidated Balance Sheets at September 30, 2016.
(d)
Approximately 16.7kr billion of borrowings under a 25kr billion facility with nine Swedish and foreign banks that matures on August 30,October 2017, and accordingly is included in current portion of long-term debt and other long-term obligations in the Condensed Consolidated Balance Sheets at September 30, 2016. At September 30, 2016, includes a fair value adjustment of approximately $192 million.

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(e)
Represents a bank loan of 2kr billion with AB Svensk Exportkredit (publ), as lender (“Svensk Exportkredit”) which is callable by the lender as a result of the completion of the Offer,March 31, 2017 and accordingly is included in current portion of long-term debt and other long-term obligations in the Condensed Consolidated Balance Sheets at September 30,December 31, 2016.
(f)(b) 
The 20142016 Term Loan maturesLoans mature on December 19, 2017.November 22, 2019 and bear interest at LIBOR (determined in accordance with the 2016 Term Credit Agreement) plus 1.375% per annum. At March 31, 2017, the weighted average interest rate of the 2016 Term Loans was approximately 2.35%.
(g)(c) 
Swedish medium term notes (“MTN”) program with an upper limit of 7kr billion. Of the total amount outstanding of 1.35kr1.3kr billion, 600kr588.0kr million matures on April 5, 2018 and 750kr745.0kr million matures on May 21, 2019. At March 31, 2017, the weighted average interest rate of the MTNs was approximately 2.01%.
(h)(d)
Instrument bears interest at a rate of three-month EURIBOR plus 0.870% per annum, reset quarterly.
(e) 
Instrument is callable by the Company at any time at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.30% plus, in each case, accrued and unpaid interest.
(i)(f) 
Instrument is callable by the Company at any time at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.25% plus, in each case, accrued and unpaid interest.

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(j)(g) 
Instrument is callable by the Company at any time at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.20% plus, in each case, accrued and unpaid interest.
(k)(h)
Instrument is callable by the Company at any time prior to the date that is one month prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted to the redemption date on an annual basis, at a rate equal to the applicable Bund Rate (as defined in the Euro Notes Indenture), plus 0.30% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(i) 
Instrument is callable by the Company at any time prior to the date that is one month prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.35% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(l)(j) 
Instrument is callable by the Company at any time prior to the date that is one month prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.30% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(m)(k) 
Instrument is callable by the Company at any time prior to August 29, 2023 at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.25% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(l)
Instrument is callable by the Company at any time prior to the date that is two months prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted to the redemption date on an annual basis, at a rate equal to the applicable Bund Rate (as defined in the Euro Notes Indenture), plus 0.35% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(m)
Instrument is callable by the Company at any time prior to the date that is three months prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.35% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(n) 
Instrument is callable by the Company at any time prior to the date that is three months prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted to the redemption date on an annual basis, at a rate equal to the U.S. Treasury rateapplicable Bund Rate (as defined in the Euro Notes Indenture), plus 0.35%0.45% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(o) 
Instrument is callable by the Company at any time prior to May 29, 2043 at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.25% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
(p) 
Instrument is callable by the Company at any time prior to the date that is six months prior to the instrument’s maturity date at the greater of 100% of the principal amount and the sum of the present values of the remaining scheduled payments of principal and interest discounted at the U.S. Treasury rate plus 0.40% plus, in each case, accrued and unpaid interest. On or after such date, the instrument is callable by the Company at 100% of the principal amount plus accrued and unpaid interest.
*
Instrument was issued by Mylan Inc.
**  
Instrument was issued by Mylan N.V.
Meda Borrowings
Upon settlement of the Offer on August 5, 2016, Meda became a controlled subsidiary of Mylan. Meda is party to certain debt obligations, all of which remained outstanding following the settlement of the Offer. During the three months ended September 30, 2016, the Company repaid approximately $567 million of Meda’s bank loans. Meda’s outstanding debt obligations and committed bank facilities contained change of control provisions that were triggered upon settlement of the Offer. Meda’s debt financing includes approximately 16.7kr billion of borrowings under a syndicated bank facility of 25kr billion with nine Swedish and foreign banks. This financing is augmented with borrowings via a Swedish MTN program with an upper limit of 7kr billion, a Swedish commercial paper program with an upper limit of 4kr billion and a bilateral bank loan of 2kr billion.

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The settlement of the Offer constituted a change of control under the Facilities Agreement, dated as of December 17, 2014 (as amended on October 29, 2015, the “Facilities Agreement”), among Meda, as borrower, the lenders party thereto (the “Lenders”) and Danske Bank A/S, as agent (“Danske”). As of September 30, 2016, there was $1.94 billion aggregate principal amount of loans outstanding under the Facilities Agreement. On August 30, 2016, Meda entered into the Amendment and Waiver Letter (the “Amendment”) to the Facilities Agreement, between Meda, as borrower, and Danske Bank A/S, as agent on behalf of the Lenders. The Amendment provides that (i) the lenders under the Facilities Agreement waive any put rights arising in connection with the Company’s acquisition of a majority of the issued share capital in Meda or any action taken in connection therewith; (ii) the termination date in respect of each of the loans and commitments under the Facilities Agreement will be August 30, 2017; and (iii) a change of control will occur under the Facilities Agreement if (a) the Company fails to, directly or indirectly, own all or substantially all of the issued share capital or votes in Meda or (b) any person (other than Stichting Preferred Shares Mylan) acquires more than 50% of the issued share capital or votes in the Company. Of the total facility amount of 25kr billion, the Company has available approximately 7.9kr billion ($925.1 million) of uncommitted borrowings at September 30, 2016.
The settlement of the Offer constituted a change of control under the terms of the notes issued by Meda under its MTN program. In accordance with the terms of the notes, Meda notified the noteholders of the occurrence of the change of control on August 5, 2016. As of September 30, 2016, there was $157.5 million aggregate principal amount of notes outstanding under the MTN program. As a result of such change of control, each noteholder had an individual right (a “put right”) to demand early redemption of the notes at their principal amount, together with accrued interest up to and including the date of redemption. The date of redemption for the notes of the noteholders that chose to exercise their put rights was November 3, 2016 and approximately $2.0 million was paid on that date.
The settlement of the Offer constituted a Change of Control (as defined in the Loan Agreement referred to below) under the Loan Agreement, dated as of September 17, 2014 (the “Loan Agreement”), between Meda, as borrower, and Svensk Exportkredit, as lender. As of September 30, 2016, there was $233.3 million aggregate principal amount of loans outstanding under the Loan Agreement. In accordance with the terms of the Loan Agreement, Meda notified Svensk Exportkredit of the Change of Control. No agreement to amend the terms of the Loan Agreement was reached within 30 days of Svensk Exportkredit’s receipt of notice from Meda of the Change of Control. Svensk Exportkredit may cancel its commitment and demand repayment of the loans under the Loan Agreement by notice to Meda, with repayment to be made not less than 30 days after such notice to Meda. The loans under the Loan Agreement will be repaid in accordance with the terms thereof.
The Facilities Agreement contains customary affirmative covenants, including among others, covenants pertaining to the delivery of financial statements, notices of default and certain material events, maintenance of authorizations, property, and insurance and compliance with laws, as well as customary negative covenants, including limitations on the incurrence of subsidiary indebtedness, disposals, loans and guarantees, liens, mergers and certain other corporate reconstructions, acquisitions and changes in Meda’s lines of business. Pursuant to the Facilities Agreement, Meda must deliver to Danske (i) within 60 days after the end of each consecutive three month period of its financial years, its unaudited consolidated financial statements for such three month period and (ii) within 120 days after the end of each of its financial years, its audited consolidated financial statements for such financial year. The Facilities Agreement contains financial covenants limited to (i) a maximum senior net debt to EBITDA ratio and (ii) a minimum EBITDA interest coverage ratio.
The MTN program contains covenants that, among other things, restrict Meda's ability and the ability of certain of Meda's subsidiaries to substantially change the general nature of its business; create liens to secure debt securities or other publicly traded debt; or sell or dispose of Meda's assets to the extent such sales or disposition could jeopardize Meda’s ability to fulfill its obligations under the MTN program; and require Meda to maintain the listing of the loans under the MTN program on Nasdaq Stockholm. As long as the loans under the MTN program are listed on Nasdaq Stockholm, Meda is required to comply with certain Nasdaq Stockholm financial reporting requirements. The MTN program also provides for customary events of default (subject in certain cases to customary grace and cure periods), which include nonpayment, breach of covenants, payment defaults or acceleration of other indebtedness, failure to pay certain judgments and certain events of bankruptcy and insolvency. These covenants and events of default are subject to a number of important qualifications, limitations and exceptions that are described in the general terms and conditions of the MTN program. If an event of default with respect to the loans under the MTN program occurs, the principal amount of all of the loans under the MTN program then outstanding, plus accrued and unpaid interest, if any, to the date of acceleration, may become immediately due and payable.
The Loan Agreement contains customary affirmative covenants, including among others, covenants pertaining to the delivery of financial statements, notices of default and certain material events, maintenance of authorizations and compliance with laws, as well as customary negative covenants, including limitations on the incurrence of subsidiary indebtedness,

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disposals, liens, mergers and certain other corporate reconstructions and changes in Meda’s lines of business. Pursuant to the Loan Agreement, Meda must deliver to Svensk Exportkredit (i) within 60 days after the end of each consecutive three month period of its financial years, its unaudited consolidated financial statements for such three month period and (ii) within 120 days after the end of each of its financial years, its audited consolidated financial statements for such financial year. The Loan Agreement contains financial covenants limited to (i) a maximum senior net debt to EBITDA ratio, (ii) a maximum senior net debt to equity ratio and (iii) a minimum EBITDA interest coverage ratio.
Receivables Facility
The Receivables Facility has a committed balance of $400 million, although from time-to-time, the available amount of the Receivables Facility may be less than $400 million based on accounts receivable concentration limits and other eligibility requirements. As of September 30, 2016 and December 31, 2015, the Company had no short-term borrowings under the Receivables Facility in the Condensed Consolidated Balance Sheets.
Issuance of June 2016 Senior Notes
During the second quarter of 2016, in anticipation of the completion of the Offer, Mylan N.V. issued $1.00 billion aggregate principal amount of 2.500% Senior Notes due 2019, $2.25 billion aggregate principal amount of 3.150% Senior Notes due 2021, $2.25 billion aggregate principal amount of 3.950% Senior Notes due 2026 and $1.00 billion aggregate principal amount of 5.250% Senior Notes due 2046 (collectively, the “June 2016 Senior Notes”) in a private offering exempt from the registration requirements of the Securities Act of 1933, as amended (the “Securities Act”), to qualified institutional buyers in accordance with Rule 144A and to persons outside of the U.S. pursuant to Regulation S under the Securities Act. The June 2016 Senior Notes were issued pursuant to an indenture, dated as of June 9, 2016 (the “Indenture”), among the Company, Mylan Inc., as guarantor (the “Guarantor”), and The Bank of New York Mellon, as trustee. The June 2016 Senior Notes were guaranteed by Mylan Inc. upon issuance. In addition, the Company entered into a registration rights agreement, dated as of June 9, 2016, pursuant to which the Company and Mylan Inc. will use commercially reasonable efforts to file a registration statement with respect to an offer to exchange each series of the June 2016 Senior Notes for new notes with the same aggregate principal amount and terms identical in all material respects and to cause the exchange offer registration statement to be declared effective by the SEC and to consummate the exchange offer not later than 365 days following the date of issuance of the June 2016 Senior Notes.
The Indenture contains covenants that, among other things, restrict the Company’s ability and the ability of certain of its subsidiaries to enter into sale and leaseback transactions; create liens; consolidate, merge or sell all or substantially all of the Company’s assets; and with respect to such subsidiaries only, guarantee certain of our or our other subsidiaries’ outstanding obligations or incur certain obligations without also guaranteeing our obligations under the June 2016 Senior Notes on a senior basis. The Indenture also provides for customary events of default (subject in certain cases to customary grace and cure periods), which include nonpayment, breach of covenants, payment defaults or acceleration of other indebtedness, failure to pay certain judgments and certain events of bankruptcy and insolvency. These covenants and events of default are subject to a number of important qualifications, limitations and exceptions that are described in the Indenture. If an event of default with respect to the June 2016 Senior Notes of a series occurs under the Indenture, the principal amount of all of the June 2016 Senior Notes of such series then outstanding, plus accrued and unpaid interest, if any, to the date of acceleration, may become immediately due and payable.
The 2.500% Senior Notes due 2019 mature on June 7, 2019, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 2.500% Senior Notes due 2019 bear interest at a rate of 2.500% per annum, accruing from June 9, 2016. Interest on the 2.500% Senior Notes due 2019 is payable semi-annually in arrears on June 7 and December 7 of each year, commencing on December 7, 2016. The 3.150% Senior Notes due 2021 mature on June 15, 2021, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 3.150% Senior Notes due 2021 bear interest at a rate of 3.150% per annum, accruing from June 9, 2016. Interest on the 3.150% Senior Notes due 2021 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016. The 3.950% Senior Notes due 2026 mature on June 15, 2026, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 3.950% Senior Notes due 2026 bear interest at a rate of 3.950% per annum, accruing from June 9, 2016. Interest on the 3.950% Senior Notes due 2026 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016. The 5.250% Senior Notes due 2046 mature on June 15, 2046, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 5.250% Senior Notes due 2046 bear interest at a rate of 5.250% per annum, accruing from June 9, 2016. Interest of the 5.250% Senior Notes due 2046 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016.

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At September 30, 2016, the outstanding balanceeligibility requirements. As of the 2.500% Senior Notes due 2019, 3.150% Senior Notes due 2021, 3.950% Senior Notes due 2026March 31, 2017 and 5.250% Senior Notes due 2046 was $999.0 million, $2.25 billion, $2.23 billion and $999.8 million, respectively, which includes discounts of $1.0 million, $2.5 million, $16.9 million and $0.2 million, respectively. During the nine months ended September 30,December 31, 2016, the Company incurred approximately $47.9 million in financing fees, which were recorded as deferred financing costshad no short-term borrowings under the Receivables Facility in the Condensed Consolidated Balance Sheets.
2016 BridgeRevolving Credit Agreement
In connection with the Offer, on February 10,On November 22, 2016, the Company entered into a Bridge Credit Agreementrevolving credit agreement (the “2016 BridgeRevolving Credit Agreement”), among the Company, as borrower, Mylan Inc., as a guarantor Deutsche(the “Guarantor”), certain lenders and issuing banks and Bank AG Cayman Islands Branch,of America, N.A., as the administrative agent and(in such capacity, the “Revolving Administrative Agent”). The 2016 Revolving Credit Agreement contains a lender, Goldman Sachs Bank USA, as a lender, Goldman Sachs Lending Partners LLC, as a lender, and other lenders party thereto from timerevolving credit facility (the “2016 Revolving Facility”) under which the Company may obtain extensions of credit in an aggregate principal amount not to time. The Company incurred total financing and ticking fees of approximately $45.2 million relatedexceed $2.0 billion, subject to the 2016 Bridge Credit Agreement. Duringsatisfaction of customary conditions, in U.S. Dollars or alternative currencies including Euro, Sterling, Yen and any other currency that is approved by the first quarter of 2016, the Company wrote off approximately $3.0 million of financing fees related to the Tranche B Loans (as defined in the 2016 Bridge Credit Agreement) in conjunction with the termination of the Tranche B Loans. The remaining commitmentsRevolving Administrative Agent and each lender under the 2016 Bridge Credit Agreement were permanently terminated in their entirety in connection with the completion of the offering of the JuneRevolving Facility. The 2016 Senior Notes. As a result of the termination of the 2016 Bridge Credit Agreement, the Company expensed the remaining $30.2 million of unamortized financing fees related to the 2016 Bridge Credit Agreement to other expense, net in the Condensed Consolidated Statements of Operationsduring the second quarter of 2016.
Revolving Facility
On December 19, 2014, the Company entered into a revolving credit agreement, which was amended on May 1, 2015, and further amended on June 19, 2015 and October 28, 2015 (the “Revolving Credit Agreement”) with a syndicate of lenders, which contains a $1.65 billion revolving facility (the “Revolving Facility”), which expires on December 19, 2019. The Revolving Facility includes a $150$200 million subfacility for the issuance of letters of credit and a $125$175 million subfacilitysublimit for swingline borrowings.
At September 30, 2016 and December 31, 2015, the Company had no amounts outstanding under the Revolving Facility. The current interest rate under the 2016 Revolving Facility is LIBOR (determined in accordance with the 2016 Revolving Credit Agreement) plus 1.325%1.200% per annum, if the Company chooses to make LIBOR borrowings, or at a base rate (determined in accordance with the 2016 Revolving Credit Agreement) plus 0.200% per annum. In addition, the 2016 Revolving Facility has a facility fee which is currently 0.175%. of the daily amount of the aggregate revolving commitments. The applicable margins over LIBOR and the base rate for the 2016 Revolving Facility can fluctuate based on the long term unsecured senior, non-credit enhanced debt rating of the Company by S&P Global Ratings. Moody’s Investors Service, Inc. and Fitch Ratings, Inc.
2015Amounts drawn on the 2016 Revolving Facility become due and payable on November 22, 2021 and may be voluntarily prepaid without penalty or premium, other than customary breakage costs related to prepayments of LIBOR borrowings. At March 31, 2017 and December 31, 2016, the Company had no amounts outstanding under the 2016 Revolving Facility.
2016 Term LoansCredit Agreement
On July 15, 2015,November 22, 2016, the Company entered into a term loan credit agreement which was amended on October 28, 2015 (the “2015“2016 Term Credit Agreement”) withamong the Company, as borrower, the Guarantor, as a syndicate ofguarantor, certain lenders which provided for a term loan credit facility underand Goldman Sachs Bank USA, as administrative agent pursuant to which the Company obtainedborrowed $2.0 billion in term loans denominated in the aggregate amount of $1.6 billion, consisting of (i) a closing date term loan in the amount of $1.0 billion, borrowed on July 15, 2015 and (ii) a delayed draw term loan in the amount of $600.0 million, borrowed on September 15, 2015 (collectively, the “2015U.S. dollars (the “2016 Term Loans”).
The 20152016 Term Loans mature on July 15, 2017, subject to extension to December 19, 2017. The loans under the 2015 Term Credit Agreementcurrently bear interest at LIBOR (determined in accordance with the 20152016 Term Credit Agreement) plus 1.375% per annum.
2014 Term Loan
On December 19, 2014,annum, if the Company entered intochooses to make LIBOR borrowings, or at a term credit agreement, which was amended on May 1, 2015, and further amended on October 28, 2015 (the “2014base rate (determined in accordance with the 2016 Term Credit Agreement”), with a syndicateAgreement) plus 0.375% per annum. The applicable margins over LIBOR and the base rate for the 2016 Term Loans can fluctuate based on the long term unsecured senior, non-credit enhanced debt rating of lenders which provided an $800 million term loan (the “2014the Company by the S&P Global Ratings, Moody’s Investors Service, Inc. and Fitch Ratings, Inc.
The 2016 Term Loan”). The 2014 Term Loan maturesLoans mature on December 19, 2017November 22, 2019 and hashave no required amortization payments. The 2014 Term Loan bears interest at LIBOR (determined in accordance withentire principal amount on the 2014 Term Credit Agreement) plus 1.375% per annum.
Amendment to the Revolving Credit Facility, 20152016 Term Loans will be due and 2014payable on November 22, 2019. The 2016 Term LoanLoans may be voluntary prepaid without penalty or premium, other than customary breakage costs related to prepayments of LIBOR borrowings. The Company voluntarily prepaid $400 million of the aggregate principal amount of the 2016 Term Loans in the fourth quarter of 2016 and $550 million in the first quarter of 2017. As such, at March 31, 2017, the Company had an aggregate principal amount of $1.05 billion outstanding under the 2016 Term Loans. As a result of the voluntary prepayment, the Company expensed approximately $1.9 million of deferred financing costs during the three months ended March 31, 2017.
Euro Notes
On FebruaryNovember 22, 2016, the Company completed its offering of the Floating Rate Euro Notes, the 2020 Euro Notes, the 2024 Euro Notes and the 2028 Euro Notes pursuant to the indenture dated November 22, 2016 (the “Euro Notes Indenture”) among the Company, Mylan Inc. (the “Borrower”) entered into (i) Amendment No. 3 (the “Revolving Amendment”) to the Revolving Credit Agreement, among the Borrower, the Company, certain lenders and issuing banks and Bank of America, N.A., as administrativeguarantor, and Citibank N.A., London Branch, as trustee, paying agent, (ii) Amendment No. 2 (the “2015 Term Amendment”)transfer agent, registrar and calculation agent. The Floating Rate Euro Notes, the 2020 Euro Notes, 2024 Euro Notes and 2028 Euro Notes, together, are referred to as the 2015 Term Credit Agreement, among the Borrower, the Company, certain lenders and PNC Bank, National Association, as administrative agent and (iii) Amendment No. 3 (the “2014 Term Amendment”) to the 2014 Term Credit Agreement, among the“Euro Notes.”

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Borrower,At March 31, 2017, the outstanding balance of the Floating Rate Euro Notes, 2020 Euro Notes, 2024 Euro Notes and 2028 Euro Notes was approximately $532.8 million, $796.0 million, $1,062.8 million and $791.3 million, respectively, converted at the March 31, 2017 EUR to USD spot exchange rate. At March 31, 2017, discounts on the 2020 Euro Notes, 2024 Euro Notes and 2028 Euro Notes were approximately $3.1 million, $2.7 million and $7.9 million, respectively, converted at the March 31, 2017 EUR to USD spot exchange rate. During the three months ended March 31, 2017, the Company certain lendersrecorded mark-to-market losses related to the Floating Rate Euro Notes, 2020 Euro Notes, 2024 Euro Notes and Bank2028 Euro Notes of America, N.A., as administrative agent. The Revolving Amendment, 2015 Term Amendmentapproximately $6.8 million, $10.2 million, $13.6 million and 2014 Term Amendment provide that the Company’s acquisition of Meda constitutes a Qualified Acquisition (as defined in each$10.2 million, respectively. Refer to Note 11 Financial Instruments and Risk Management for further discussion of the Revolving Credit Agreement, the 2014 Term Credit Agreement and the 2015 Term Credit Agreement) and amends the eventforeign currency risk management of default provisions to provide that any “change of control” put rights under any indebtedness of any Acquired Entity or Business (as defined in each of the Revolving Credit Agreement, the 2014 Term Credit Agreement and the 2015 Term Credit Agreement) or its subsidiaries that are triggered as a result of the acquisition of any Acquired Entity or Business will not result in an event of default so long as any such indebtedness that is put in accordance with the terms of such indebtedness is paid as required by the terms of such indebtedness.these instruments.
Fair Value
At September 30, 2016March 31, 2017 and December 31, 2015,2016, the fair value of the Company’s 1.350% Senior Notes due 2016, 2.600% Senior Notes due 2018, 3.000% Senior Notes due 2018, 2.500% Senior Notes due 2019, 2.550% Senior Notes due 2019, 3.750% Senior Notes due 2020, 3.150% Senior Notes due 2021, 3.125% Senior Notes due 2023, 4.200% Senior Notes due 2023, 3.950% Senior Notes due 2026, 5.400% Senior Notes due 2043 and 5.250% Senior Notes due 2046 (collectively, the “Senior Notes”) and Euro Notes was approximately $11.19$13.7 billion and $4.80$13.2 billion, respectively. The fair values of the Senior Notes and Euro Notes were valued at quoted market prices from broker or dealer quotations and were classified as Level 2 in the fair value hierarchy. Based on quoted market rates of interest and maturity schedules of similar debt issues, the fair values of the Company’s 20152016 Term Loans 2014 Term Loan and the Meda borrowings, determined based on Level 2 inputs, approximate their carrying values at September 30, 2016March 31, 2017 and December 31, 2015.2016.
Mandatory minimum repayments remaining on the notional amount of outstanding long-term debt at September 30, 2016, excluding the discounts, premiums and associated derivatives,March 31, 2017 are as follows for each of the periods ending December 31:
(In millions)TotalTotal
2016$733.3
20174,150.5
$223
20181,220.0
1,748
20191,587.5
2,633
2020500.0
1,299
20212,250
Thereafter7,250.0
6,865
Total$15,441.3
$15,018
13.Comprehensive Earnings
Accumulated other comprehensive loss, as reflected on the Condensed Consolidated Balance Sheets, is comprised of the following:
(In millions)September 30,
2016
 December 31,
2015
March 31,
2017
 December 31,
2016
Accumulated other comprehensive loss:      
Net unrealized gain (loss) on marketable securities, net of tax$19.5
 $(1.0)
Net unrealized gain on marketable securities, net of tax$19.4
 $14.5
Net unrecognized losses and prior service cost related to defined benefit plans, net of tax(15.1) (14.9)(0.3) (0.5)
Net unrecognized losses on derivatives in cash flow hedging relationships, net of tax(31.9) (18.1)(17.3) (38.6)
Net unrecognized losses on derivatives in net investment hedging relationships, net of tax(8.1) 
(11.3) (1.4)
Foreign currency translation adjustment(1,084.8) (1,730.3)(1,803.5) (2,237.7)
$(1,120.4) $(1,764.3)$(1,813.0) $(2,263.7)


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Components of accumulated other comprehensive loss, before tax, consist of the following, for the three and nine months ended September 30, 2016March 31, 2017 and 2015:2016:
Three Months Ended September 30, 2016Three Months Ended March 31, 2017
Gains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Net Investment Hedges Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment TotalsGains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Net Investment Hedges Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment Totals
(In millions)Foreign Currency Forward Contracts Interest Rate Swaps Total          Foreign Currency Forward Contracts Interest Rate Swaps Total          
Balance at June 30, 2016 net of tax    $(46.7) $
 $6.0
 $(15.2) $(1,375.4) $(1,431.3)
Balance at December 31, 2016, net of tax    $(38.6) $(1.4) $14.5
 $(0.5) $(2,237.7) $(2,263.7)
Other comprehensive earnings (loss) before reclassifications, before tax    9.8
 (10.4) 21.5
 (0.2) 290.6
 311.3
    25.4
 (9.9) 7.7
 (0.3) 434.2
 457.1
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:                              
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales10.7
   10.7
         10.7
5.2
   5.2
         5.2
Loss on interest rate swaps classified as cash flow hedges, included in interest expense  2.3
 2.3
         2.3
  1.8
 1.8
         1.8
Amortization of prior service costs included in SG&A          
   
          0.1
   0.1
Amortization of actuarial loss included in SG&A          0.3
   0.3
          0.2
   0.2
Net other comprehensive earnings (loss), before tax    22.8
 (10.4) 21.5
 0.1
 290.6
 324.6
    32.4
 (9.9) 7.7
 
 434.2
 464.4
Income tax provision (benefit)    8.0
 (2.3) 8.0
 
 
 13.7
    11.1
 
 2.8
 (0.2) 
 13.7
Balance at September 30, 2016, net of tax    $(31.9) $(8.1) $19.5
 $(15.1) $(1,084.8) $(1,120.4)
Balance at March 31, 2017, net of tax    $(17.3) $(11.3) $19.4
 $(0.3) $(1,803.5) $(1,813.0)



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Nine Months Ended September 30, 2016Three Months Ended March 31, 2016
Gains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Net Investment Hedges Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment TotalsGains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment Totals
Foreign Currency Forward Contracts Interest Rate Swaps Total          
(In millions)Foreign Currency Forward Contracts Interest Rate Swaps Total        
Balance at December 31, 2015, net of tax    $(18.1) $
 $(1.0) $(14.9) $(1,730.3) $(1,764.3)    $(18.1) $(1.0) $(14.9) $(1,730.3) $(1,764.3)
Other comprehensive (loss) earnings before reclassifications, before tax    (63.7) (10.4) 32.5
 (1.2) 645.5
 602.7
    (39.4) 4.4
 (0.6) 502.0
 466.4
Amounts reclassified from accumulated other comprehensive (loss) earnings, before tax:                            
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales34.2
   34.2
         34.2
(10.6)   (10.6)       (10.6)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense  6.6
 6.6
         6.6
Gain on interest rate swaps classified as cash flow hedges, included in interest expense  0.9
 0.9
       0.9
Amortization of prior service costs included in SG&A          0.2
   0.2
        0.1
   0.1
Amortization of actuarial loss included in SG&A          0.7
   0.7
Amortization of actuarial gain included in SG&A        0.2
   0.2
Net other comprehensive (loss) earnings, before tax    (22.9) (10.4) 32.5
 (0.3) 645.5
 644.4
    (49.1) 4.4
 (0.3) 502.0
 457.0
Income tax (benefit) provision    (9.1) (2.3) 12.0
 (0.1) 
 0.5
    (18.3) 1.6
 (0.1) 
 (16.8)
Balance at September 30, 2016, net of tax    $(31.9) $(8.1) $19.5
 $(15.1) $(1,084.8) $(1,120.4)
Balance at March 31, 2016, net of tax    $(48.9) $1.8
 $(15.1) $(1,228.3) $(1,290.5)


14.Shareholders’ Equity
A summary of the changes in shareholders’ equity for the three months endedMarch 31, 2017 and 2016 is as follows:
(In millions)Total
Mylan N.V.
Shareholders' Equity
 Noncontrolling Interest Total
December 31, 2016$11,116.2
 $1.4
 $11,117.6
Net earnings66.4
 
 66.4
Other comprehensive earnings, net of tax450.7
 
 450.7
Stock option activity5.2
 
 5.2
Share-based compensation expense23.1
 
 23.1
Issuance of restricted stock, net of shares withheld(5.6) 
 (5.6)
Other
 (1.4) (1.4)
March 31, 2017$11,656.0
 $
 $11,656.0


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 Three Months Ended September 30, 2015
Gains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment Totals
(In millions)Foreign Currency Forward Contracts Interest Rate Swaps Total        
Balance at June 30, 2015, net of tax    $(17.6) $0.1
 $(16.4) $(1,317.7) $(1,351.6)
Other comprehensive (loss) earnings before reclassifications, before tax    (92.5) (0.2) 0.1
 (148.4) (241.0)
Amounts reclassified from accumulated other comprehensive (loss) earnings, before tax:             
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales(8.1)   (8.1)       (8.1)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense  (0.2) (0.2)       (0.2)
Amortization of actuarial gain included in SG&A        0.1
   0.1
Amounts reclassified from accumulated other comprehensive loss, before tax    (8.3) 
 0.1
 
 (8.2)
Net other comprehensive loss, before tax    (84.2) (0.2) 
 (148.4) (232.8)
Income tax (benefit) provision    (30.8) (0.2) 0.2
 
 (30.8)
Balance at September 30, 2015, net of tax    $(71.0) $0.1
 $(16.6) $(1,466.1) $(1,553.6)


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 Nine Months Ended September 30, 2015
 Gains and Losses on Derivatives in Cash Flow Hedging Relationships Gains and Losses on Marketable Securities Defined Pension Plan Items Foreign Currency Translation Adjustment Totals
 Foreign Currency Forward Contracts Interest Rate Swaps Total        
Balance at December 31, 2014, net of tax    $(28.4) $0.3
 $(19.5) $(939.4) $(987.0)
Other comprehensive (loss) earnings before reclassifications, before tax    (98.3) (0.4) 4.5
 (526.7) (620.9)
Amounts reclassified from accumulated other comprehensive loss, before tax:             
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales(30.4)   (30.4)       (30.4)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense  (0.5) (0.5)       (0.5)
Amortization of prior service costs included in SG&A        0.2
   0.2
Amortization of actuarial gain included in SG&A        0.4
   0.4
Amounts reclassified from accumulated other comprehensive loss, before tax    (30.9) 
 0.6
 
 (30.3)
Net other comprehensive (loss) earnings, before tax    (67.4) (0.4) 3.9
 (526.7) (590.6)
Income tax (benefit) provision    (24.8) (0.2) 1.0
 
 (24.0)
Balance at September 30, 2015, net of tax    $(71.0) $0.1
 $(16.6) $(1,466.1) $(1,553.6)
14.Shareholders’ Equity
A summary of the changes in shareholders’ equity for the nine months endedSeptember 30, 2016 and 2015 is as follows:
(In millions)Total Mylan N.V. Shareholders' Equity Noncontrolling Interest Total
December 31, 2015$9,764.4
 $1.4
 $9,765.8
Net earnings62.5
 
 62.5
Other comprehensive earnings, net of tax643.9
 
 643.9
Stock option activity11.1
 
 11.1
Share-based compensation expense71.1
 
 71.1
Issuance of restricted stock, net of shares withheld(9.6) 
 (9.6)
Tax benefit of stock option plans2.2
 
 2.2
Issuance of ordinary shares to purchase Meda1,281.7
 
 1,281.7
Other
 0.1
 0.1
September 30, 2016$11,827.3
 $1.5
 $11,828.8


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(In millions)Total Mylan N.V. Shareholders' Equity Noncontrolling Interest Total
December 31, 2014$3,255.9
 $20.1
 $3,276.0
Net earnings653.0
 0.1
 653.1
Other comprehensive loss, net of tax(566.6) 
 (566.6)
Stock option activity92.9
 
 92.9
Share-based compensation expense66.4
 
 66.4
Issuance of restricted stock, net of shares withheld(41.5) 
 (41.5)
Tax benefit of stock option plans49.5
 
 49.5
Issuance of ordinary shares to purchase the EPD Business6,305.8
 
 6,305.8
Purchase of subsidiary shares from noncontrolling interest
 (18.7) (18.7)
Other(1.8) (0.1) (1.9)
September 30, 2015$9,813.6
 $1.4
 $9,815.0
On August 5, 2016, in conjunction with the Offer, the Company issued approximately 26.4 million Mylan N.V. ordinary shares to Meda shareholders. On February 27, 2015, as part of the EPD Transaction, the Company acquired the EPD Business from Abbott Laboratories in exchange for 110 million ordinary shares of Mylan N.V.
On April 3, 2015, the Company and Stichting Preferred Shares Mylan (the “Foundation”) entered into a call option agreement (the “Call Option Agreement”). Pursuant to the terms of the Call Option Agreement, Mylan N.V. granted the Foundation a call option (the “Option”), permitting the Foundation to acquire from time-to-time Mylan N.V. preferred shares up to a maximum number equal to the total number of Mylan N.V. ordinary shares issued at such time to the extent such shares are not held by the Foundation. In response to Teva Pharmaceutical Industries Ltd.’s (“Teva”) unsolicited expression of interest to acquire Mylan on July 23, 2015, the Foundation exercised the Option and acquired 488,388,431 Mylan preferred shares pursuant to the terms of the Call Option Agreement. Each Mylan ordinary share and preferred share was entitled to one vote on each matter properly brought before a general meeting of shareholders. On July 27, 2015, Teva announced its entry into an agreement to acquire the Generic Drug Unit of Allergan plc and the withdrawal of its unsolicited, non-binding expression of interest to acquire Mylan. On September 19, 2015, the Foundation requested the redemption of the Mylan preferred shares issued. Mylan ordinary shareholders approved the redemption of the preferred shares on January 7, 2016 at an extraordinary general meeting of shareholders and on March 17, 2016, the redemption of the Mylan preferred shares became effective. The Foundation will continue to have the right to exercise the Option in the future in response to a new threat to the interests of Mylan, its businesses and its stakeholders from time to time.
With effect from February 27, 2015, the general meeting authorized the board to repurchase Company shares for a maximum period of 18 months, with such authorization expiring on August 27, 2016 (the “Share Repurchase Authorization”). More specifically, the general meeting authorized the board to repurchase the maximum number of ordinary shares allowed under Dutch law and applicable securities regulations on the NASDAQ for a period of 18 months. On June 24, 2016, at the annual general meeting, the Company’s shareholders approved an extension of the Share Repurchase Authorization, which will now expire on December 24, 2017. On July 27, 2016, the board approved the commensurate extension of the Share Repurchase Program (as defined below).
On November 16, 2015, the Company announced that its board of directors approved the repurchase of up to $1.0 billion of the Company’s ordinary shares either in the open market through privately-negotiated transactions or in one of more self tender offers (the “Share Repurchase Program”). At September 30, 2016, the Share Repurchase Program has approximately $932.5 million remaining for ordinary share repurchases. The Share Repurchase Program does not obligate the Company to acquire any particular amount of ordinary shares.
(In millions)Total
Mylan N.V.
Shareholders' Equity
 Noncontrolling Interest Total
December 31, 2015$9,764.4
 $1.4
 $9,765.8
Net earnings13.9
 
 13.9
Other comprehensive earnings, net of tax473.8
 
 473.8
Stock option activity3.5
 
 3.5
Share-based compensation expense26.5
 
 26.5
Issuance of restricted stock, net of shares withheld(9.9) 
 (9.9)
Tax benefit of stock option plans1.2
 
 1.2
Other
 0.1
 0.1
March 31, 2016$10,273.4
 $1.5
 $10,274.9
15.Segment Information
As a result of our acquisition of Meda and the integration of our portfolio across our branded, generics and over-the-counter (“OTC”) platforms in all of our regions, effective October 1, 2016, the Company expanded its reportable segments. The Company has twothree reportable segments “Generics”on a geographic basis as follows: North America, Europe and “Specialty.” The GenericsRest of World. Our North America segment is made up of our operations in the U.S. and Canada and includes the operations of our previously reported Specialty segment. Our Europe segment is made up of our operations in 35 countries within the region. Our Rest of World segment is primarily develops, manufactures, sellsmade up of our operations in India, Australia, Japan and distributes generic or branded generic pharmaceutical productsNew Zealand. Also included in tablet, capsule, injectable, transdermal patch, gel, cream or ointment form,our Rest of World segment are our operations in emerging markets, which includes countries in Africa (including South Africa) as well as active pharmaceutical ingredients (“API”). The SpecialtyBrazil and other countries throughout Asia and the Middle East. Comparative segment

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Notes financial information has been recast for prior periods to Condensed Consolidated Financial Statements (Unaudited) - Continued


engages mainly in the development and sale of branded specialty nebulized and injectable products. Meda operations have been included in the Genericsconform to this revised segment for the three and nine months ended September 30, 2016.reporting.
The Company’s chief operating decision maker is the Chief Executive Officer, who evaluates the performance of the Company’sits segments based on total revenues and segment profitability. Segment profitability represents segment gross profit less direct R&D expenses and direct SG&A.&A expenses. Certain general and administrative and R&D expenses not allocated to the segments, net charges for litigation settlements and other contingencies, impairment charges and other expenses not directly attributable to the segments and certain intercompany transactions, including eliminations, are reported in Corporate/Other. Additionally, amortization of intangible assets and other purchase accounting related items, as well as anycertain other significant special items, are included in Corporate/Other. Items below the earnings from operations line on the Company’s Condensed Consolidated Statements of Operations are not presented by segment, since they are excluded from the measure of segment profitability. The Company does not report depreciation expense, total assets and capital expenditures by segment, as such information is not used by the chief operating decision maker.
The accounting policies of the segments are the same as those described in the “Summary of Significant Accounting Policies” included in Mylan N.V.’s Annual Report on Form 10-K for the year ended December 31, 2015,2016, as amended. Intersegment revenues are accounted for at current market values and are eliminated at the consolidated level.
Due to our acquisition of Meda on August 5, 2016 and the integration of our portfolio across our branded, generics and OTC platforms in all of our regions, effective October 1, 2016, the Company is expanding its reportable segments. The Company will report its results in three segments on a geographic basis as follows: (1) North America, (2) Europe and (3) Rest of World. This change in segment reporting will begin with the Company’s consolidated financial statements for the year ending December 31, 2016. Comparative segment financial information will be recast for prior periods to conform to this revised segment structure. Identifiable intangible assets and goodwill previously allocated to the Generics and Specialty Segments will be reallocated to the new segments. The Company’s measure of segment profitability will remain unchanged.
Presented in the table below is segment information for the periods identified and a reconciliation of segment information to total consolidated information.
(In millions) Generics Segment Specialty Segment 
Corporate /
Other
(1)
 Consolidated
Three Months Ended September 30, 2016       
Total revenues       
Third party$2,625.0
 $432.1
 $
 $3,057.1
Intersegment27.4
 7.2
 (34.6) 
Total$2,652.4
 $439.3
 $(34.6) $3,057.1
        
Segment profitability (loss)$799.3
 $278.2
 $(1,208.2) $(130.7)
         
Nine Months Ended September 30, 2016     
Total revenues       
Third party$6,709.4
 $1,099.7
 $
 $7,809.1
Intersegment29.5
 13.7
 (43.2) 
Total$6,738.9
 $1,113.4
 $(43.2) $7,809.1
        
Segment profitability$1,923.7
 $658.3
 $(2,196.2) $385.8
(In millions)North America Europe Rest of World Corporate /
Other
 Consolidated
Three Months Ended March 31, 2017         
Third party net sales$1,214.9
 $892.0
 $580.5
 $
 $2,687.4
Other revenue23.4
 6.7
 2.0
 
 32.1
Intersegment13.1
 42.9
 99.1
 (155.1) 
Total$1,251.4
 $941.6
 $681.6
 $(155.1) $2,719.5
          
Segment profitability$589.7
 $233.8
 $76.6
 $(672.9) $227.2

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(In millions)(In millions) Generics Segment Specialty Segment 
Corporate /
Other
(1)
 ConsolidatedNorth America Europe Rest of World Corporate /
Other
 Consolidated
Three Months Ended September 30, 2015       
Total revenues       
Third party$2,249.9
 $445.3
 $
 $2,695.2
Three Months Ended March 31, 2016         
Third party net sales$1,157.5
 $584.3
 $434.3
 $
 $2,176.1
Other revenue14.0
 0.3
 1.1
 
 15.2
IntersegmentIntersegment1.4
 1.2
 (2.6) 
6.3
 25.2
 85.1
 (116.6) 
TotalTotal$2,251.3
 $446.5
 $(2.6) $2,695.2
$1,177.8
 $609.6
 $520.5
 $(116.6) $2,191.3
                 
Segment profitabilitySegment profitability$788.5
 $258.2
 $(445.6) $601.1
$573.8
 $124.6
 $29.6
 $(622.4) $105.6
        
Nine Months Ended September 30, 2015       
Total revenues       
Third party$5,968.8
 $969.8
 $
 $6,938.6
Intersegment5.2
 5.8
 (11.0) 
Total$5,974.0
 $975.6
 $(11.0) $6,938.6
        
Segment profitability$1,834.0
 $524.2
 $(1,321.2) $1,037.0
____________
(1)
Includes certain corporate general and administrative and R&D expenses; litigation settlements and other contingencies, net, which for the three and nine months ended September 30, 2016 included the Medicaid Drug Rebate Program Settlement and the Strides Settlement, as discussed further in Note 18 Contingencies; certain intercompany transactions, including eliminations; amortization of intangible assets and certain purchase accounting items; impairment charges; and other expenses not directly attributable to segments.
16.Subsidiary Guarantors
The following tables present unaudited condensed consolidating financial information for (a) Mylan N.V., the Company (for purposesissuer of this discussionthe 3.000% Senior Notes due 2018, 2.500% Senior Notes due 2019, 3.750% Senior Notes due 2020, 3.150% Senior Notes due 2021, 3.950% Senior Notes due 2026 and these tables, “Parent Guarantor”5.250% Senior Notes due 2046 (collectively, the “Mylan N.V. Senior Notes”), which are guaranteed on a senior unsecured basis by Mylan Inc.; (b) Mylan Inc., the issuer of certainthe 2.600% Senior Notes (fordue 2018, 2.550% Senior Notes due 2019, 3.125% Senior Notes due 2023, 4.200% Senior Notes due 2023 and 5.400% Senior Notes due 2043 (collectively, the purposes of this discussion and these tables, the “Issuer”) (Refer to Note 12Debt for further discussion of the“Mylan Inc. Senior Note issuances)Notes”), which are guaranteed on a senior unsecured basis by Mylan N.V.; and (c) all other subsidiaries of the Parent GuarantorCompany on a combined basis, none of which guaranteedguarantee the Cash ConvertibleMylan N.V. Senior Notes or guarantee the Mylan Inc. Senior Notes (“Non-Guarantor Subsidiaries”). The consolidating adjustments primarily relate to eliminations of investments in subsidiaries and intercompany balances and transactions. The unaudited condensed consolidating financial statements present investments in subsidiaries using the equity method of accounting. Mylan Inc. is an indirect wholly owned subsidiary of the Company and the Company fully and unconditionally guaranteed on a senior unsecured basis the Senior Notes issued by Mylan Inc.

In addition, the Company’s 3.000% Senior Notes due December 2018 and the 3.750% Senior Notes due December 2020 (collectively, the “December 2015 Senior Notes”) and June 2016 Senior Notes are guaranteed on a senior unsecured basis by Mylan Inc. In connection with the offering of the December 2015 Senior Notes and June 2016 Senior Notes, the Company entered into separate registration rights agreements pursuant to which the Company and Mylan Inc. will use commercially reasonable efforts to file a registration statement with respect to an offer to exchange each series of the December 2015 Senior Notes and June 2016 Senior Notes for new notes with the same aggregate principal amount and terms substantially identical in all material respects and to cause the exchange offer registration statement to be declared effective by the SEC and to consummate the exchange offer not later than 365 days following the respective dates of issuance of the December 2015 Senior Notes and the June 2016 Senior Notes.
The following financial information presents the related unaudited Condensed Consolidating Statements of Operations for the three and nine months ended September 30,March 31, 2017 and 2016, and 2015, the unaudited Condensed Consolidating Statements of Comprehensive Earnings for the three and nine months ended September 30,March 31, 2017 and 2016, and 2015, the unaudited Condensed Consolidating Balance Sheets as of September 30, 2016March 31, 2017 and December 31, 20152016 and the unaudited Condensed Consolidating Statements of Cash Flows for the ninethree months ended September 30, 2016March 31, 2017 and 2015.2016. This unaudited condensed consolidating financial information has been prepared and presented in accordance with SEC Regulation S-X Rule 3-10 “Financial Statements of Guarantors and Issuers of Guaranteed Securities Registered or Being Registered.”

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS
Three Months Ended September 30, 2016March 31, 2017
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Revenues:                      
Net sales$
 $
 $
 $3,029.5
 $
 $3,029.5
$
 $
 $
 $2,687.4
 $
 $2,687.4
Other revenues
 
 
 27.6
 
 27.6

 
 
 32.1
 
 32.1
Total revenues
 
 
 3,057.1
 
 3,057.1

 
 
 2,719.5
 
 2,719.5
Cost of sales
 
 
 1,773.8
 
 1,773.8

 
 
 1,634.5
 
 1,634.5
Gross profit
 
 
 1,283.3
 
 1,283.3

 
 
 1,085.0
 
 1,085.0
Operating expenses:                      
Research and development
 
 
 199.1
 
 199.1

 
 
 217.5
 
 217.5
Selling, general and administrative43.1
 134.0
 
 479.8
 
 656.9
12.6
 156.5
 
 462.2
 
 631.3
Litigation settlements and other contingencies, net
 
 
 558.0
 
 558.0

 
 
 9.0
 
 9.0
Total operating expenses43.1
 134.0
 
 1,236.9
 
 1,414.0
12.6
 156.5
 
 688.7
 
 857.8
(Losses) earnings from operations(43.1) (134.0) 
 46.4
 
 (130.7)(12.6) (156.5) 
 396.3
 
 227.2
Interest expense70.7
 40.9
 
 32.8
 
 144.4
97.6
 25.4
 
 15.2
 
 138.2
Other (income) expense, net(31.4) (102.7) 
 184.3
 
 50.2
(95.5) (57.3) 
 170.2
 
 17.4
(Loss) earnings before income taxes(82.4) (72.2) 
 (170.7) 
 (325.3)(14.7) (124.6) 
 210.9
 
 71.6
Income tax provision (benefit)
 8.1
 
 (213.6) 
 (205.5)(1.6) 3.2
 
 3.6
 
 5.2
Earnings (loss) of equity interest subsidiaries(37.4) 442.9
 
 
 (405.5) 
79.5
 214.0
 
 
 (293.5) 
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders$(119.8) $362.6
 $
 $42.9
 $(405.5) $(119.8)
Net earnings$66.4
 $86.2
 $
 $207.3
 $(293.5) $66.4


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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS
Nine Months Ended September 30, 2016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Revenues:           
Net sales$
 $
 $
 $7,745.5
 $
 $7,745.5
Other revenues
 
 
 63.6
 
 63.6
Total revenues
 
 
 7,809.1
 
 7,809.1
Cost of sales
 
 
 4,447.1
 
 4,447.1
Gross profit
 
 
 3,362.0
 
 3,362.0
Operating expenses:           
Research and development
 
 
 632.2
 
 632.2
Selling, general and administrative75.8
 499.2
 
 1,212.6
 
 1,787.6
Litigation settlements and other contingencies, net
 
 
 556.4
 
 556.4
Total operating expenses75.8
 499.2
 
 2,401.2
 
 2,976.2
(Loss) earnings from operations(75.8) (499.2) 
 960.8
 
 385.8
Interest expense115.1
 126.3
 
 63.6
 
 305.0
Other expense (income), net53.6
 (305.7) 
 436.1
 
 184.0
(Loss) earnings before income taxes(244.5) (319.8) 
 461.1
 
 (103.2)
Income tax provision (benefit)
 22.1
 
 (187.8) 
 (165.7)
Earnings of equity interest subsidiaries307.0
 1,055.7
 
 
 (1,362.7) 
Net earnings attributable to Mylan N.V. ordinary shareholders$62.5
 $713.8
 $
 $648.9
 $(1,362.7) $62.5

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS
Three Months Ended September 30, 2015March 31, 2016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Revenues:                      
Net sales$
 $
 $
 $2,676.2
 $
 $2,676.2
$
 $
 $
 $2,176.1
 $
 $2,176.1
Other revenues
 
 
 19.0
 
 19.0

 
 
 15.2
 
 15.2
Total revenues
 
 
 2,695.2
 
 2,695.2

 
 
 2,191.3
 
 2,191.3
Cost of sales
 
 
 1,379.9
 
 1,379.9

 
 
 1,284.3
 
 1,284.3
Gross profit
 
 
 1,315.3
 
 1,315.3

 
 
 907.0
 
 907.0
Operating expenses:                      
Research and development
 
 
 174.8
 
 174.8

 
 
 253.6
 
 253.6
Selling, general and administrative
 193.9
 
 343.2
 
 537.1
13.2
 176.0
 
 360.1
 
 549.3
Litigation settlements and other contingencies, net
 
 
 2.3
 
 2.3

 
 
 (1.5) 
 (1.5)
Total operating expenses
 193.9
 
 520.3
 
 714.2
13.2
 176.0
 
 612.2
 
 801.4
(Losses) earnings from operations
 (193.9) 
 795.0
 
 601.1
(13.2) (176.0) 
 294.8
 
 105.6
Interest expense30.4
 49.4
 
 15.3
 
 95.1
13.3
 41.5
 
 15.5
 
 70.3
Other expense, net
 
 
 50.9
 
 50.9

 
 
 16.3
 
 16.3
Earnings from operations(30.4) (243.3) 
 728.8
 
 455.1
Income tax (benefit) provision
 (46.4) 
 72.9
 
 26.5
(Losses) earnings from operations(26.5) (217.5) 
 263.0
 
 19.0
Income tax provision (benefit)
 9.0
 
 (3.9) 
 5.1
Earnings of equity interest subsidiaries459.0
 643.0
 
 
 (1,102.0) 
40.4
 264.8
 
 
 (305.2) 
Net earnings428.6
 446.1
 
 655.9
 (1,102.0) 428.6
$13.9
 $38.3
 $
 $266.9
 $(305.2) $13.9
Net earnings attributable to noncontrolling interest
 
 
 
 
 
Net earnings attributable to Mylan N.V. ordinary shareholders$428.6
 $446.1
 $
 $655.9
 $(1,102.0) $428.6

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF OPERATIONS
Nine Months Ended September 30, 2015
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Revenues:           
Net sales$
 $
 $
 $6,887.8
 $
 $6,887.8
Other revenues
 
 
 50.8
 
 50.8
Total revenues
 
 
 6,938.6
 
 6,938.6
Cost of sales
 
 
 3,785.1
 
 3,785.1
Gross profit
 
 
 3,153.5
 
 3,153.5
Operating expenses:           
Research and development
 
 
 512.9
 
 512.9
Selling, general and administrative
 611.0
 
 973.5
 
 1,584.5
Litigation settlements and other contingencies, net
 
 
 19.1
 
 19.1
Total operating expenses
 611.0
 
 1,505.5
 
 2,116.5
(Losses) earnings from operations
 (611.0) 
 1,648.0
 
 1,037.0
Interest expense42.3
 179.7
 
 46.5
 
 268.5
Other expense, net
 
 
 71.4
 
 71.4
(Loss) earnings before income taxes(42.3) (790.7) 
 1,530.1
 
 697.1
Income tax (benefit) provision
 (88.2) 
 132.2
 
 44.0
Earnings of equity interest subsidiaries695.4
 1,391.3
 
 
 (2,086.7) 
Net earnings653.1
 688.8
 
 1,397.9
 (2,086.7) 653.1
Net earnings attributable to noncontrolling interest(0.1) 
 
 (0.1) 0.1
 (0.1)
Net earnings attributable to Mylan N.V. ordinary shareholders$653.0
 $688.8
 $
 $1,397.8
 $(2,086.6) $653.0


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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF COMPREHENSIVE EARNINGS
Three Months Ended September 30, 2016March 31, 2017
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Net (loss) earnings$(119.8) $362.6
 $
 $42.9
 $(405.5) $(119.8)
Net earnings$66.4
 $86.2
 $
 $207.3
 $(293.5) $66.4
Other comprehensive earnings (loss), before tax:                      
Foreign currency translation adjustment290.6
 1.5
 
 289.0
 (290.5) 290.6
434.2
 
 
 434.2
 (434.2) 434.2
Change in unrecognized gain (loss) and prior service cost related to defined benefit plans0.1
 0.2
 
 (0.1) (0.1) 0.1

 0.1
 
 (0.1) 
 
Net unrecognized gain on derivatives in cash flow hedging relationships22.8
 2.3
 
 20.5
 (22.8) 22.8
32.4
 1.8
 
 30.6
 (32.4) 32.4
Net unrecognized loss on derivatives in net investment hedging relationships(10.4) 
 
 (10.4) 10.4
 (10.4)(9.9) 
 
 (9.9) 9.9
 (9.9)
Net unrealized gain (loss) on marketable securities21.5
 21.5
 
 (0.1) (21.4) 21.5
7.7
 7.8
 
 (0.1) (7.7) 7.7
Other comprehensive earnings (loss), before tax324.6
 25.5
 
 298.9
 (324.4) 324.6
Other comprehensive earnings, before tax464.4
 9.7
 
 454.7
 (464.4) 464.4
Income tax provision13.7
 8.7
 
 3.9
 (12.6) 13.7
13.7
 (3.6) 
 17.3
 (13.7) 13.7
Other comprehensive earnings, net of tax310.9
 16.8
 
 295.0
 (311.8) 310.9
450.7
 13.3
 
 437.4
 (450.7) 450.7
Comprehensive (loss) earnings191.1
 379.4
 
 337.9
 (717.3) 191.1
Comprehensive earnings attributable to the noncontrolling interest
 
 
 
 
 
Comprehensive earnings (loss) attributable to Mylan N.V. ordinary shareholders$191.1
 $379.4
 $
 $337.9
 $(717.3) $191.1
Comprehensive earnings (loss)$517.1
 $99.5
 $
 $644.7
 $(744.2) $517.1


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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF COMPREHENSIVE EARNINGS
Nine Months Ended September 30, 2016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Net earnings$62.5
 $713.8
 $
 $648.9
 $(1,362.7) $62.5
Other comprehensive earnings (loss), before tax:           
Foreign currency translation adjustment645.5
 
 
 645.5
 (645.5) 645.5
Change in unrecognized (loss) gain and prior service cost related to defined benefit plans(0.3) 0.2
 
 (0.6) 0.4
 (0.3)
Net unrecognized (loss) gain on derivatives in cash flow hedging relationships(22.9) (49.8) 
 26.9
 22.9
 (22.9)
Net unrealized loss on derivatives in net investment hedging relationships(10.4) 
 
 (10.4) 10.4
 (10.4)
Net unrealized gain on marketable securities32.5
 31.5
 
 0.9
 (32.4) 32.5
Other comprehensive earnings (loss), before tax644.4
 (18.1) 
 662.3
 (644.2) 644.4
Income tax provision (benefit)0.5
 (6.8) 
 6.3
 0.5
 0.5
Other comprehensive earnings (loss), net of tax643.9
 (11.3) 
 656.0
 (644.7) 643.9
Comprehensive earnings (loss)706.4
 702.5
 
 1,304.9
 (2,007.4) 706.4
Comprehensive earnings attributable to the noncontrolling interest
 
 
 
 
 
Comprehensive earnings attributable to Mylan N.V. ordinary shareholders$706.4
 $702.5
 $
 $1,304.9
 $(2,007.4) $706.4

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF COMPREHENSIVE EARNINGS
Three Months Ended September 30, 2015March 31, 2016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Net (loss) earnings$428.6
 $446.1
 $
 $655.9
 $(1,102.0) $428.6
Other comprehensive loss, before tax:           
Foreign currency translation adjustment(148.4) 
 
 (148.4) 148.4
 (148.4)
Change in unrecognized gain and prior service cost related to defined benefit plans
 0.2
 
 (0.2) 
 
Net unrecognized gain (loss) on derivatives(84.2) (63.9) 
 (20.3) 84.2
 (84.2)
Net unrealized loss on marketable securities(0.2) 
 
 (0.2) 0.2
 (0.2)
Other comprehensive loss, before tax(232.8) (63.7) 
 (169.1) 232.8
 (232.8)
Income tax benefit(30.8) (23.8) 
 (7.0) 30.8
 (30.8)
Other comprehensive loss, net of tax(202.0) (39.9) 
 (162.1) 202.0
 (202.0)
Comprehensive earnings226.6
 406.2
 
 493.8
 (900.0) 226.6
Comprehensive earnings attributable to the noncontrolling interest
 
 
 
 
 
Comprehensive earnings attributable to Mylan N.V. ordinary shareholders$226.6
 $406.2
 $
 $493.8
 $(900.0) $226.6
(In millions)Mylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Net earnings$13.9
 $38.3
 $
 $266.9
 $(305.2) $13.9
Other comprehensive earnings (loss), before tax:           
Foreign currency translation adjustment502.0
 
 
 502.0
 (502.0) 502.0
Change in unrecognized (loss) gain and prior service cost related to defined benefit plans(0.3) 
 
 (0.3) 0.3
 (0.3)
Net unrecognized (loss) gain on derivatives(49.1) (58.4) 
 9.3
 49.1
 (49.1)
Net unrealized gain on marketable securities4.4
 3.8
 
 0.6
 (4.4) 4.4
Other comprehensive earnings (loss), before tax457.0
 (54.6) 
 511.6
 (457.0) 457.0
Income tax (benefit) provision(16.8) (20.2) 
 3.4
 16.8
 (16.8)
Other comprehensive earnings (loss), net of tax473.8
 (34.4) 
 508.2
 (473.8) 473.8
Comprehensive earnings$487.7
 $3.9
 $
 $775.1
 $(779.0) $487.7


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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF COMPREHENSIVE EARNINGS
Nine Months Ended September 30, 2015
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Net (loss) earnings$653.1
 $688.8
 $
 $1,397.9
 $(2,086.7) $653.1
Other comprehensive earnings (loss), before tax:           
Foreign currency translation adjustment(526.7) 
 
 (526.7) 526.7
 (526.7)
Change in unrecognized gain and prior service cost related to defined benefit plans3.9
 0.3
 
 3.6
 (3.9) 3.9
Net unrecognized loss on derivatives(67.4) (57.7) 
 (9.7) 67.4
 (67.4)
Net unrealized loss on marketable securities(0.4) 
 
 (0.4) 0.4
 (0.4)
Other comprehensive loss, before tax(590.6) (57.4) 
 (533.2) 590.6
 (590.6)
Income tax benefit(24.0) (21.1) 
 (2.9) 24.0
 (24.0)
Other comprehensive loss, net of tax(566.6) (36.3) 
 (530.3) 566.6
 (566.6)
Comprehensive earnings86.5
 652.5
 
 867.6
 (1,520.1) 86.5
Comprehensive earnings attributable to the noncontrolling interest(0.1) 
 
 (0.1) 0.1
 (0.1)
Comprehensive earnings attributable to Mylan N.V. ordinary shareholders$86.4
 $652.5
 $
 $867.5
 $(1,520.0) $86.4

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING BALANCE SHEET
As of September 30, 2016March 31, 2017
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
ASSETS                      
Assets                      
Current assets:                      
Cash and cash equivalents$
 $33.2
 $
 $1,223.4
 $
 $1,256.6
$
 $6.3
 $
 $717.5
 $
 $723.8
Accounts receivable, net
 7.4
 
 3,091.5
 
 3,098.9

 5.4
 
 2,866.6
 
 2,872.0
Inventories
 
 
 2,687.5
 
 2,687.5

 
 
 2,547.8
 
 2,547.8
Intercompany receivables165.8
 420.8
 
 10,019.0
 (10,605.6) 
220.1
 427.3
 
 11,317.7
 (11,965.1) 
Prepaid expenses and other current assets1.5
 256.7
 
 663.9
 
 922.1
6.4
 245.9
 
 669.6
 
 921.9
Total current assets167.3
 718.1
 
 17,685.3
 (10,605.6) 7,965.1
226.5
 684.9
 
 18,119.2
 (11,965.1) 7,065.5
Property, plant and equipment, net
 331.3
 
 1,952.9
 
 2,284.2

 351.9
 
 1,986.1
 
 2,338.0
Investments in subsidiaries17,755.5
 9,912.6
 
 
 (27,668.1) 
16,047.7
 8,589.3
 
 
 (24,637.0) 
Intercompany notes and interest receivable2,268.9
 10,054.4
 
 18.7
 (12,342.0) 
7,555.4
 9,928.1
 
 16.7
 (17,500.2) 
Intangible assets, net
 
 
 15,613.4
 
 15,613.4

 
 
 14,370.0
 
 14,370.0
Goodwill
 17.1
 
 9,616.0
 
 9,633.1

 17.1
 
 9,377.0
 
 9,394.1
Other assets
 97.1
 
 945.6
 
 1,042.7
5.3
 37.4
 
 1,062.3
 
 1,105.0
Total assets$20,191.7
 $21,130.6
 $
 $45,831.9
 $(50,615.7) $36,538.5
$23,834.9
 $19,608.7
 $
 $44,931.3
 $(54,102.3) $34,272.6
                      
LIABILITIES AND EQUITY                      
Liabilities                      
Current liabilities:                      
Trade accounts payable$
 $30.0
 $
 $1,224.9
 $
 $1,254.9
$0.5
 $38.5
 $
 $1,102.4
 $
 $1,141.4
Short-term borrowings
 
 
 54.2
 
 54.2

 
 
 31.0
 
 31.0
Income taxes payable
 33.2
 
 131.3
 
 164.5

 
 
 31.0
 
 31.0
Current portion of long-term debt and other long-term obligations
 2,188.2
 
 2,246.4
 
 4,434.6

 0.2
 
 294.2
 
 294.4
Intercompany payables420.8
 10,184.8
 
 
 (10,605.6) 
427.3
 11,537.8
 
 
 (11,965.1) 
Other current liabilities514.3
 309.2
 
 2,822.3
 
 3,645.8
102.7
 354.3
 
 2,569.4
 
 3,026.4
Total current liabilities935.1
 12,745.4
 
 6,479.1
 (10,605.6) 9,554.0
530.5
 11,930.8
 
 4,028.0
 (11,965.1) 4,524.2
Long-term debt7,427.8
 3,735.7
 
 165.1
 
 11,328.6
11,648.4
 2,896.7
 
 155.7
 
 14,700.8
Intercompany notes payable
 1,466.5
 
 10,875.4
 (12,341.9) 

 3,449.4
 
 14,050.8
 (17,500.2) 
Other long-term obligations
 55.3
 
 3,771.8
 
 3,827.1

 57.9
 
 3,333.7
 
 3,391.6
Total liabilities8,362.9
 18,002.9
 
 21,291.4
 (22,947.5) 24,709.7
12,178.9
 18,334.8
 
 21,568.2
 (29,465.3) 22,616.6
                      
Total equity11,828.8
 3,127.7
 
 24,540.5
 (27,668.2) 11,828.8
11,656.0
 1,273.9
 
 23,363.1
 (24,637.0) 11,656.0
                      
Total liabilities and equity$20,191.7
 $21,130.6
 $
 $45,831.9
 $(50,615.7) $36,538.5
$23,834.9
 $19,608.7
 $
 $44,931.3
 $(54,102.3) $34,272.6

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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING BALANCE SHEET
As of December 31, 20152016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
ASSETS                      
Assets                      
Current assets:                      
Cash and cash equivalents$
 $870.5
 $
 $365.5
 $
 $1,236.0
$0.3
 $12.3
 $
 $986.2
 $
 $998.8
Accounts receivable, net
 14.4
 
 2,674.7
 
 2,689.1

 12.3
 
 3,298.6
 
 3,310.9
Inventories
 
 
 1,951.0
 
 1,951.0

 
 
 2,456.4
 
 2,456.4
Intercompany receivables1,097.5
 283.2
 
 8,936.4
 (10,317.1) 
215.9
 416.0
 
 10,506.6
 (11,138.5) 
Other current assets0.3
 244.8
 
 351.5
 
 596.6
Prepaid expenses and other current assets
 256.4
 
 500.0
 
 756.4
Total current assets1,097.8
 1,412.9
 
 14,279.1
 (10,317.1) 6,472.7
216.2
 697.0
 
 17,747.8
 (11,138.5) 7,522.5
Property, plant and equipment, net
 324.4
 
 1,659.5
 
 1,983.9

 360.3
 
 1,961.9
 
 2,322.2
Investments in subsidiaries9,947.7
 8,007.7
 
 
 (17,955.4) 
15,606.2
 8,277.8
 
 
 (23,884.0) 
Intercompany notes and interest receivable
 9,704.4
 
 18.7
 (9,723.1) 
7,952.3
 9,817.3
 
 16.7
 (17,786.3) 
Intangible assets, net
 0.5
 
 7,221.4
 
 7,221.9

 
 
 14,447.8
 
 14,447.8
Goodwill
 17.1
 
 5,363.0
 
 5,380.1

 17.1
 
 9,214.8
 
 9,231.9
Other assets
 135.3
 
 1,073.8
 
 1,209.1
5.2
 51.9
 
 1,144.7
 
 1,201.8
Total assets$11,045.5
 $19,602.3
 $
 $29,615.5
 $(37,995.6) $22,267.7
$23,779.9
 $19,221.4
 $
 $44,533.7
 $(52,808.8) $34,726.2
                      
LIABILITIES AND EQUITY                      
Liabilities                      
Current liabilities:                      
Trade accounts payable$
 $33.5
 $
 $1,076.1
 $
 $1,109.6
$3.9
 $69.6
 $
 $1,274.6
 $
 $1,348.1
Short-term borrowings
 
 
 1.3
 
 1.3

 
 
 46.4
 
 46.4
Income taxes payable
 
 
 92.4
 
 92.4

 
 
 97.7
 
 97.7
Current portion of long-term debt and other long-term obligations
 1,010.1
 
 66.9
 
 1,077.0

 0.2
 
 289.8
 
 290.0
Intercompany payables283.2
 10,033.9
 
 
 (10,317.1) 
416.0
 10,722.5
 
 
 (11,138.5) 
Other current liabilities2.0
 320.1
 
 1,519.8
 
 1,841.9
90.9
 388.8
 
 2,778.8
 
 3,258.5
Total current liabilities285.2
 11,397.6
 
 2,756.5
 (10,317.1) 4,122.2
510.8
 11,181.1
 
 4,487.3
 (11,138.5) 5,040.7
Long-term debt994.5
 5,298.4
 
 2.7
 
 6,295.6
12,151.5
 2,897.6
 
 153.8
 
 15,202.9
Intercompany notes payable
 18.7
 
 9,704.4
 (9,723.1) 

 3,870.9
 
 13,915.4
 (17,786.3) 
Other long-term obligations
 122.2
 
 1,961.9
 
 2,084.1

 58.1
 
 3,306.9
 
 3,365.0
Total liabilities1,279.7
 16,836.9
 
 14,425.5
 (20,040.2) 12,501.9
12,662.3
 18,007.7
 
 21,863.4
 (28,924.8) 23,608.6
                      
Total equity9,765.8
 2,765.4
 
 15,190.0
 (17,955.4) 9,765.8
11,117.6
 1,213.7
 
 22,670.3
 (23,884.0) 11,117.6
                      
Total liabilities and equity$11,045.5
 $19,602.3
 $
 $29,615.5
 $(37,995.6) $22,267.7
$23,779.9
 $19,221.4
 $
 $44,533.7
 $(52,808.8) $34,726.2

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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF CASH FLOWS
NineThree Months Ended September 30, 2016March 31, 2017
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Cash flows from operating activities:                      
Net cash (used in) provided by operating activities$(1.6) $724.7
 $
 $974.6
 $
 $1,697.7
$(27.4) $(192.7) $
 $673.0
 $
 $452.9
Cash flows from investing activities:                      
Capital expenditures
 (64.8) 
 (174.7) 
 (239.5)
 (18.3) 
 (40.1) 
 (58.4)
Change in restricted cash
 (49.5) 
 (1.0) 
 (50.5)
 
 
 12.7
 
 12.7
Purchase of marketable securities
 (4.1) 
 (18.7) 
 (22.8)
 
 
 (2.3) 
 (2.3)
Cash paid for Meda's unconditional deferred payment
 
 
 (308.0) 
 (308.0)
Proceeds from sale of assets
 
 
 31.1
 
 31.1
Proceeds from sale of marketable securities
 
 
 15.8
 
 15.8

 
 
 2.3
 
 2.3
Cash paid for acquisitions, net(5,278.5) (931.3) 
 58.1
 
 (6,151.7)(71.6) 
 
 
 
 (71.6)
Settlement of acquisition-related foreign currency derivatives(128.6) 
 
 
 
 (128.6)
Investments in affiliates
 (43.6) 
 
 43.6
 

 (7.2) 
 
 7.2
 
Dividends from affiliates135.6
 
 
 
 (135.6) 
52.4
 
 
 
 (52.4) 
Loans to affiliates(7,971.9) (417.0) 
 (726.3) 9,115.2
 
(100.2) (111.1) 
 (977.5) 1,188.8
 
Repayments of loans from affiliates6,838.3
 442.6
 
 1,031.3
 (8,312.2) 
701.3
 0.3
 
 188.8
 (890.4) 
Payments for product rights and other, net
 (0.4) 
 (195.9) 
 (196.3)
 (0.1) 
 (77.8) 
 (77.9)
Net cash (used in) provided by investing activities(6,405.1) (1,068.1) 
 (319.4) 711.0
 (7,081.6)581.9
 (136.4) 
 (862.8) 253.2
 (164.1)
Cash flows from financing activities:                      
Payments of financing fees(95.3) 
 
 
 
 (95.3)(3.7) 
 
 
 
 (3.7)
Change in short-term borrowings, net
 
 
 48.6
 
 48.6

 
 
 (17.6) 
 (17.6)
Proceeds from issuance of long-term debt6,478.8
 
 
 41.0
 
 6,519.8
Payments of long-term debt
 (500.0) 
 (567.0) 
 (1,067.0)(550.0) 
 
 
 
 (550.0)
Proceeds from exercise of stock options11.1
 
 
 
 
 11.1
5.0
 
 
 
 
 5.0
Taxes paid related to net share settlement of equity awards(12.9) 
 
 
 
 (12.9)(6.1) 
 
 
 
 (6.1)
Contingent consideration payments
 
 
 (15.5) 
 (15.5)
 
 
 (3.8) 
 (3.8)
Capital contribution from affiliates
 
 
 43.6
 (43.6) 

 
 
 7.2
 (7.2) 
Capital payments to affiliates
 
 
 (135.6) 135.6
 

 
 
 (52.4) 52.4
 
Payments on borrowings from affiliates
 (1,361.8) 
 (6,950.4) 8,312.2
 

 (648.3) 
 (242.1) 890.4
 
Proceeds from borrowings from affiliates25.0
 1,380.8
 
 7,709.4
 (9,115.2) 

 977.5
 
 211.3
 (1,188.8) 
Acquisition of noncontrolling interest
 
 
 (1.0) 
 (1.0)
Other items, net
 (12.9) 
 14.5
 
 1.6

 (6.1) 
 6.6
 
 0.5
Net cash provided by financing activities6,406.7
 (493.9) 
 187.6
 (711.0) 5,389.4
(554.8) 323.1
 
 (90.8) (253.2) (575.7)
Effect on cash of changes in exchange rates
 
 
 15.1
 
 15.1

 
 
 11.9
 
 11.9
Net (decrease) increase in cash and cash equivalents
 (837.3) 
 857.9
 
 20.6
(0.3) (6.0) 
 (268.7) 
 (275.0)
Cash and cash equivalents — beginning of period
 870.5
 
 365.5
 
 1,236.0
0.3
 12.3
 
 986.2
 
 998.8
Cash and cash equivalents — end of period$
 $33.2
 $
 $1,223.4
 $
 $1,256.6
$
 $6.3
 $
 $717.5
 $
 $723.8
Supplemental disclosures of cash flow information —           
Non-cash transactions:           
Ordinary shares issued for acquisition$1,281.7
 $
 $
 $
 $
 $1,281.7

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MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


UNAUDITED CONDENSED CONSOLIDATING STATEMENT OF CASH FLOWS
NineThree Months Ended September 30, 2015March 31, 2016
(In millions)Mylan N.V. (Parent Guarantor) Mylan Inc. (Issuer) Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations ConsolidatedMylan N.V. Mylan Inc. Guarantor Subsidiaries Non-Guarantor Subsidiaries Eliminations Consolidated
Cash flows from operating activities:                      
Net cash (used in) provided by operating activities$
 $(1,417.1) $
 $2,773.6
 $
 $1,356.5
$(27.1) $(139.4) $
 $247.0
 $
 $80.5
Cash flows from investing activities:                      
Capital expenditures
 (55.1) 
 (152.2) 
 (207.3)
 (20.6) 
 (31.2) 
 (51.8)
Change in restricted cash
 
 
 25.9
 
 25.9
Purchase of marketable securities
 (29.3) 
 (29.8) 
 (59.1)
 (0.5) 
 (8.0) 
 (8.5)
Proceeds from sale of marketable securities
 
 
 29.4
 
 29.4

 
 
 5.9
 
 5.9
Investments in affiliates
 (289.4) 
 
 289.4
 

 (11.3) 
 
 11.3
 
Loans to affiliates(39.5) (4,250.1) 
 (5,657.3) 9,946.9
 
(3.6) (1,465.6) 
 (1,699.6) 3,168.8
 
Repayments of loans from affiliates
 240.6
 
 22.5
 (263.1) 
32.8
 12.2
 
 7.2
 (52.2) 
Payments for product rights and other, net
 
 
 (428.2) 
 (428.2)
 (0.1) 
 (105.5) 
 (105.6)
Net cash used in investing activities(39.5) (4,383.3) 
 (6,189.7) 9,973.2
 (639.3)
Net cash provided by (used in) investing activities29.2
 (1,485.9) 
 (1,831.2) 3,127.9
 (160.0)
Cash flows from financing activities:                      
Payments of financing fees(89.1) (25.6) 
 
 
 (114.7)(31.6) 
 
 
 
 (31.6)
Change in short-term borrowings, net
 
 
 (329.7) 
 (329.7)
 
 
 65.1
 
 65.1
Proceeds from convertible note hedge
 1,970.8
 
 
 
 1,970.8
Proceeds from issuance of long-term debt
 2,390.0
 
 
 
 2,390.0
Payments of long-term debt
 (4,334.1) 
 
 
 (4,334.1)
Proceeds from exercise of stock options39.5
 53.3
 
 
 
 92.8
3.6
 
 
 
 
 3.6
Taxes paid related to net share settlement of equity awards
 (25.8) 
 (5.9) 
 (31.7)(6.9) 
 
 
 
 (6.9)
Capital contribution from affiliates
 
 
 289.4
 (289.4) 

 
 
 11.3
 (11.3) 
Payments on borrowings from affiliates
 (22.5) 
 (240.6) 263.1
 

 (40.0) 
 (12.2) 52.2
 
Proceeds from borrowings from affiliates89.1
 5,696.8
 
 4,161.0
 (9,946.9) 
31.6
 1,703.2
 
 1,434.0
 (3,168.8) 
Acquisition of noncontrolling interest
 
 
 (11.7) 
 (11.7)
Other items, net1.3
 48.3
 
 
 
 49.6
1.2
 
 
 (0.9) 
 0.3
Net cash provided by financing activities40.8
 5,751.2
 
 3,862.5
 (9,973.2) (318.7)
Net cash (used in) provided by financing activities(2.1) 1,663.2
 
 1,497.3
 (3,127.9) 30.5
Effect on cash of changes in exchange rates
 
 
 (37.0) 
 (37.0)
 
 
 12.4
 
 12.4
Net increase (decrease) in cash and cash equivalents1.3
 (49.2) 
 409.4
 
 361.5

 37.9
 
 (74.5) 
 (36.6)
Cash and cash equivalents — beginning of period0.1
 112.9
 
 112.5
 
 225.5

 870.5
 
 365.5
 
 1,236.0
Cash and cash equivalents — end of period$1.4
 $63.7
 $
 $521.9
 $
 $587.0
$
 $908.4
 $
 $291.0
 $
 $1,199.4
Supplemental disclosures of cash flow information —           
Non-cash transactions:           
Ordinary shares issued for acquisition$6,305.8
 $
 $
 $
 $
 $6,305.8

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


17.Income TaxesRestructuring
The Company computes its provision for income taxes using an estimated effective tax rate for the full year with consideration of certain discrete tax items which occurred within the interim period. During the three months ended September 30,On December 5, 2016, the Company received approvals fromannounced restructuring programs in certain locations representing initial steps in a series of actions that are anticipated to further streamline its operations globally. Since 2015, the relevant Indian regulatory authoritiesCompany has made a number of significant acquisitions, and as part of the holistic, global integration of these acquisitions, the Company is focused on how to legally mergebest optimize and maximize all of its wholly owned subsidiary, Jai Pharma Limited, into Mylan Laboratories Limited. The merger resultedassets across the organization and across all geographies.

Charges for restructuring and ongoing cost reduction initiatives are recorded in the period the Company commits to a restructuring or cost reduction plan, or executes specific actions contemplated by the plan and all criteria for liability recognition of a deferred tax asset of $150 million forhave been met.

The Company continues to develop the tax deductible goodwill in excessdetails of the book goodwillcost reduction initiatives, including workforce actions and other potential restructuring activities beyond the programs announced, including potential shutdown or consolidation of certain operations. The continued restructuring actions are expected to be implemented through fiscal year 2018. For the restructuring activities that have been initiated to date, the Company estimates that it will incur aggregate pre-tax charges ranging between $175.0 million and $225.0 million, inclusive of the 2016 and year to date 2017 restructuring charges of $172.8 million. As additional restructuring activities are undertaken, the Company expects to incur additional costs including employee related costs, such as severance and continuation of healthcare and other benefits; asset impairments; accelerated depreciation; costs associated with a corresponding benefit to income tax provision forcontract terminations; and other closure costs. At this time, the three and nine months ended September 30, 2016. In additionexpenses related to the benefit recognizedadditional restructuring activities cannot be reasonably estimated.

The following table summarizes the restructuring charges and the reserve activity from December 31, 2016 to March 31, 2017:
(In millions)Employee Related Costs Other Exit Costs Total
Balance at December 31, 2016:$138.6
 $1.6
 $140.2
Charges (1)
9.6
 13.5
 23.1
Reclassifications(8.3) 8.3
 
Cash payment(54.2) (1.0) (55.2)
Utilization
 (19.8) (19.8)
Foreign currency translation(9.8) 
 (9.8)
Balance at March 31, 2017:$75.9
 $2.6
 $78.5
____________
(1)
For the three months ended March 31, 2017, total restructuring charges in North America, Europe, Rest of World and Corporate / Other were approximately $6.4 million, $3.6 million, $12.8 millionand $0.3 million, respectively.

At March 31, 2017 and December 31, 2016, accrued liabilities for restructuring and other costs reduction programs were included in other current liabilities on the merger of the aforementioned entities, the effective tax rate for the three and nine months ended September 30, 2016 versus the three and nine months ended September 30, 2015 was also impacted by the Medicaid Drug Rebate Program Settlement.Condensed Consolidated Balance Sheets.
18.ContingenciesCollaboration and Licensing Agreements
Legal ProceedingsWe periodically enter into collaboration and licensing agreements with other pharmaceutical companies for the development, manufacture, marketing and/or sale of pharmaceutical products. Our significant collaboration agreements are focused on the development, manufacturing, supply and commercialization of multiple, high-value generic biologic compounds, insulin analog products and respiratory products. Under these agreements, we have future potential milestone payments and co-development expenses payable to third parties as part of our licensing, development and co-development programs. Payments under these agreements generally become due and are payable upon the satisfaction or achievement of certain developmental, regulatory or commercial milestones or as development expenses are incurred on defined projects. Milestone payment obligations are uncertain, including the prediction of timing and the occurrence of events triggering a future obligation and are not reflected as liabilities in the Condensed Consolidated Balance Sheets, except for milestone and royalty obligations reflected as acquisition related contingent consideration. Refer to Note 11Financial Instruments and Risk Management for contingent consideration amounts recorded. These agreements may also include potential sales-based milestones and call for us to pay a percentage of amounts earned from the sale of the product as a royalty or a profit share. The

42

Table of Contents
MYLAN N.V. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued


amounts disclosed do not include sales based milestones or royalty obligations on future sales of product as the timing and amount of future sales levels and costs to produce products subject to these obligations is not reasonably estimable. These sales-based milestones or royalty obligations may be significant depending upon the level of commercial sales for each product. There have been no significant changes to our collaboration and licensing agreements as disclosed in our Annual Report on Form 10-K for the year ended December 31, 2016, as amended.
19.Litigation
The Company is involved in various disputes, governmental and/or regulatory inquiries and proceedings, tax proceedings and litigation matters that arise from time to time, some of which are described below. The Company is also party to certain litigation matters including those for which Merck KGaA, Abbott Laboratories or Strides Arcolab has agreed to indemnify the Company, pursuant to the respective sale and purchase agreements.
While the Company believes that it has meritorious defenses with respect to the claims asserted against it and intends to vigorously defend its position, the process of resolving matters through litigation or other means is inherently uncertain, and it is not possible to predict the ultimate resolution of any such proceeding. It is possible that an unfavorable resolution of any of the matters described below, or the inability or denial of Merck KGaA, Abbott Laboratories, Strides Arcolab, or another indemnitor or insurer to pay an indemnified claim, could have a material effect on the Company’s business, financial condition, results of operations, cash flows and/or ordinary share price. Unless otherwise disclosed below, the Company is unable to predict the outcome of the respective litigation or to provide an estimate of the range of reasonably possible losses. Legal costs are recorded as incurred and are classified in SG&A in the Company’s Condensed Consolidated Statements of Operations.
Lorazepam and Clorazepate
On June 1, 2005, a jury verdict was rendered against Mylan, MPI, and co-defendants Cambrex Corporation and Gyma Laboratories in the U.S. District Court for the District of Columbia in the amount of approximately $12.0 million, which has been accrued for by the Company. The jury found that Mylan and its co-defendants willfully violated Massachusetts, Minnesota and Illinois state antitrust laws in connection with APIactive pharmaceutical ingredient supply agreements entered into between the Company and its API supplier (Cambrex) and broker (Gyma) for two drugs, Lorazepam and Clorazepate, in 1997, and subsequent price increases on these drugs in 1998. The case was brought by four health insurers who opted out of earlier class action settlements agreed to by the Company in 2001 and represents the last remaining antitrust claims relating to Mylan’s 1998 price increases for Lorazepam and Clorazepate. Following the verdict, the Company filed a motion for judgment as a matter of law, a motion for a new trial, a motion to dismiss two of the insurers and a motion to reduce the verdict. On December 20, 2006, the Company’s motion for judgment as a matter of law and motion for a new trial were denied and the remaining motions were denied on January 24, 2008. In post-trial filings, the plaintiffs requested that the verdict be trebled and that request was granted on January 24, 2008. On February 6, 2008, a judgment was issued against Mylan and its co-defendants in the total amount of approximately $69.0 million, which, in the case of three of the plaintiffs, reflects trebling of the compensatory damages in the original verdict (approximately $11.0 million in total) and, in the case of the fourth plaintiff, reflects their amount of the compensatory damages in the original jury verdict plus doubling this compensatory damage award as punitive damages assessed against each of the defendants (approximately $58.0 million in total), some or all of which may be subject to indemnification obligations by Mylan. Plaintiffs are also seeking an award of attorneys’ fees and litigation costs in unspecified amounts and prejudgment interest of approximately $8.0 million. The Company and its co-defendants appealed to the U.S. Court of Appeals for the D.C. Circuit and have challenged the verdict as legally erroneous on multiple grounds. The appeals were held in abeyance pending a ruling on the motion for prejudgment interest, which has been granted. Mylan has contested this ruling along with the liability finding and other damages awards as part of its appeal, which was filed in the Court of Appeals for the D.C. Circuit. On January 18, 2011, the Court of Appeals issued a judgment remanding the case to the District Court for further proceedings based on lack of diversity with respect to certain plaintiffs. On June 13, 2011, Mylan filed a certiorari petition with the U.S. Supreme Court requesting review of the judgment of the D.C. Circuit. On October 3, 2011, the certiorari petition was denied. The case is now proceeding before the District Court. On January 14, 2013, following limited court-ordered jurisdictional discovery, the plaintiffs filed a fourth amended complaint containing additional factual averments with respect to the diversity

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of citizenship of the parties, along with a motion to voluntarily dismiss 775 (of 1,387) self-funded customers whose presence would destroy the District Court’s diversity jurisdiction. The plaintiffs also moved for a remittitur (reduction) of approximately $8.1 million from the full damages award. Mylan’s brief in response to the new factual averments in the complaint was filed on February 13, 2013. On July 29, 2014, the court granted both plaintiffs’ motion to amend the complaint and their motion to dismiss 775 self-funded customers.

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In connection with the Company’s appeal of the judgment, the Company submitted a surety bond underwritten by a third-party insurance company in the amount of $74.5 million in February 2008. On May 30, 2012, the District Court ordered the amount of the surety bond reduced to $66.6 million.
Pricing and Medicaid Litigation
Dey L.P. (now known as Mylan Specialty L.P. and herein as “Mylan Specialty”), a wholly owned subsidiary of the Company, was named as a defendant in several class actions brought by consumers and third-party payors. Mylan Specialty reached a settlement of these class actions, which was approved by the court and all claims have been dismissed. Additionally, a complaint was filed under seal by a plaintiff on behalf of the United States of America against Mylan Specialty in August 1997. In August 2006, the Government filed its complaint-in-intervention and the case was unsealed in September 2006. The Government asserted that Mylan Specialty was jointly liable with a co-defendant and sought recovery of alleged overpayments, together with treble damages, civil penalties and equitable relief. Mylan Specialty completed a settlement of this action in December 2010. These cases all have generally alleged that Mylan Specialty falsely reported certain price information concerning certain drugs marketed by Mylan Specialty, that Mylan Specialty caused false claims to be made to Medicaid and to Medicare, and that Mylan Specialty caused Medicaid and Medicare to make overpayments on those claims.

Under the terms of the purchase agreement with Merck KGaA, Mylan is fully indemnified for the claims in the preceding paragraph and Merck KGaA is entitled to any income tax benefit the Company realizes for any deductions of amounts paid for such pricing litigation. Under the indemnity, Merck KGaA is responsible for all settlement and legal costs, and, as such, these settlements had no impact on the Company’s Consolidated Statements of Operations. At September 30, 2016March 31, 2017, the Company has accrued approximately $63.3 million in other current liabilities, which represents its estimate of the remaining amount of anticipated income tax benefits due to Merck KGaA. We are not aware of any outstanding claims related to Merck KGaA.

Modafinil Antitrust Litigation and FTC Inquiry
Beginning in April 2006, Mylan and four other drug manufacturers have been named as defendants in civil lawsuits filed in or transferred to the U.S. District Court for the Eastern District of Pennsylvania by a variety of plaintiffs purportedly representing direct and indirect purchasers of the drug modafinil and in a lawsuit filed by Apotex, Inc., a manufacturer of generic drugs. These actions allege violations of federal antitrust and state laws in connection with the generic defendants’ settlement of patent litigation with Cephalon relating to modafinil. Discovery hasis closed. On June 23, 2014, the court granted the defendants’ motion for partial summary judgment dismissing plaintiffs’ claims that the defendants had engaged in an overall conspiracy to restrain trade (and denied the corresponding plaintiffs’ motion). On January 28, 2015, the District Court denied the defendants’ summary judgment motions based on factors identified in the Supreme Court’s Actavis decision. In an order ofon June 1, 2015, vacated and reissued on June 11, 2015, the District Court denied the indirect purchaser plaintiffs’ motion for class certification. The indirect purchaser plaintiffs filed a petition for leave to appeal the certification decision, which was denied by the Court of Appeals for the Third Circuit on December 21, 2015. On July 27, 2015, the District Court granted the direct purchaser plaintiffs’ motion for class certification. On October 9, 2015, the Third Circuit granted defendants’ petition for leave to appeal the class certification decision. On October 16, 2015, defendants filed a motion to stay the liability trial, which had been set to begin on February 2, 2016, with the District Court pending the appeal of the decision to certify the direct purchaser class; this motion was denied on December 17, 2015. On December 17, 2015, the District Court approved the form and manner of notice to the certified class of direct purchasers; the notice was subsequently issued to the class. On December 21, 2015, the defendants filed a motion to stay with the Court of Appeals for the Third Circuit, which was granted on January 25, 2016; accordingly, the trial is nowwas stayed and the case has beenwas placed in suspense. The appeal was fully briefed on April 28, 2016. Oral arguments on the appeal took place on July 12, 2016. On September 13, 2016, the Third Circuit reversed the district court’s certification order and remanded for further proceedings. On October 14, 2016 direct purchaser plaintiffs filed a petition seeking rehearing. On October 31, 2016 the petition seeking rehearing was denied. On December 12, 2016, the District Court removed the case from suspense and set the trial for June 5, 2017. On March 24, 2015, Mylan reached a settlement in principle with the putative indirect purchasers, and on November 20, 2015, Mylan entered into a settlement agreement with the putative indirect purchasers.purchasers for approximately $16 million. Plaintiffs have not yet moved for preliminary approval of that settlement. At September 30,In December 2016, Mylan reached a settlement with the putative direct purchaser class and the retailer opt-out plaintiffs for $165 million, of which approximately $68.5 million was paid before December 31, 2016. The settlement with the retailer opt-out plaintiffs has been completed. The settlement with the putative direct purchaser class will undergo the court approval process. On February 3, 2017, the putative direct purchaser class moved for preliminary approval. The Company has accrued approximately $16.0$112.5 million related to this settlement.matter at March 31, 2017 and December 31, 2016.

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On June 29, 2015, the City of Providence, Rhode Island filed suit in the District of Rhode Island against the same parties named as defendants in litigation pending in the Eastern District of Pennsylvania, including Mylan, asserting state law claims based on the same underlying allegations. All defendants, including Mylan, moved to dismiss the suit on October 15, 2015, and the case was subsequently settled.
On July 10, 2015, the Louisiana Attorney General filed in the 19th Judicial District Court in Louisiana a petition against Mylan and three other drug manufacturers asserting state law claims based on the same underlying allegations as those made in litigation pending in the Eastern District of Pennsylvania. The petition was filed by the State of Louisiana purportedly in its capacity as an indirect purchaser. On May 16, 2016, the Judicial District Court deferred Mylan’s declinatory exception of no personal jurisdiction and its peremptory exception of prescription, and granted in part and denied in part Mylan’s peremptory exceptions of no cause of action and no right of action. On June 30, 2016, the plaintiff filed a supplemental and amended petition. The defendants filed a motion to strike and joint peremptory exceptions to the amended petition, which remain pending.petition. On July 21, 2016, the plaintiff filed in the First Circuit Court of Appeal its application for a supervisory writ regarding the granting of defendant’s exceptions, which the defendants have opposed. The appeal was denied on October 31, 2016. On April 20, 2016, the State of Louisiana filed a motion to consolidate the pending action with four other actions against other pharmaceutical manufacturers concerning products not related to modafinil, which Mylan opposed. On June 27, 2016, the Judicial District Court declined to consolidate Mylan’s case with the other four actions, with leave to renew the consolidation request after filing the above-referenced amended petition. On July 21, 2016, the plaintiff filed a motion to reurge consolidation. Subsequently, the action to which plaintiff seeks to join Mylan was stayed, resulting in a stay of the consolidation motion. On December 8, 2016, Mylan’s peremptory exceptions of no cause of action with respect to the supplemental and amended petition were granted in their entirety and with prejudice and judgment was entered. On February 17, 2017, the plaintiff filed in the 19th Judicial District Court a motion for appeal, which the Judicial District Court granted on February 21, 2017. The appeal was lodged with the First Circuit Court of Appeal on April 4, 2017.
On July 28, 2016, United Healthcare filed a complaint against Mylan and four other drug manufacturers in the United States District Court for the District of Minnesota, asserting state law claims based on the same underlying allegations as those made in litigation pending in the Eastern District of Pennsylvania. Mylan’s response deadlineOn January 6, 2017, the case was transferred to the Eastern District of Pennsylvania. Mylan filed its answer to the complaint on March 31, 2017.
The Company believes that it has strong defenses to these remaining cases. Although it is November 30, 2016.reasonably possible that the Company may incur additional losses from these matters, any amount cannot be reasonably estimated at this time.
In addition, by letter dated July 11, 2006, Mylan was notified by the U.S. Federal Trade Commission (“FTC”) of an investigation relating to the settlement of the modafinil patent litigation. In its letter, the FTC requested certain information from Mylan, MPI and Mylan Technologies, Inc. pertaining to the patent litigation and the settlement thereof. On March 29, 2007, the FTC issued a subpoena, and on April 26, 2007, the FTC issued a civil investigative demand to Mylan, requesting additional information from the Company relating to the investigation. Mylan has cooperated fully with the government’s investigation and completed all requests for information. On February 13, 2008, the FTC filed a lawsuit against Cephalon in the U.S. District Court for the District of Columbia and the case was subsequently transferred to the U.S. District Court for the Eastern District of Pennsylvania. On July 1, 2010, the FTC issued a third party subpoena to Mylan, requesting documents in connection with its lawsuit against Cephalon. Mylan has responded to the subpoena. The lawsuit against Cephalon settled and a Stipulated Order for Permanent Injunction and Equitable Monetary Relief was entered by the Court on June 17, 2015.
Pioglitazone
Beginning in December 2013, Mylan, Takeda, and several other drug manufacturers have been named as defendants in civil lawsuits consolidated in the U.S. District Court for the Southern District of New York by plaintiffs which purport to represent indirect purchasers of branded or generic Actos® and Actoplus Met®. These actions allege violations of state and federal competition laws in connection with the defendants’ settlements of patent litigation in 2010 relating to Actos and Actoplus Met®. Plaintiffs filed an amended complaint on August 22, 2014. Mylan and the other defendants filed motions to dismiss the amended complaint on October 10, 2014. Two additional complaints were subsequently filed by plaintiffs purporting to represent classes of direct purchasers of branded or generic Actos® and Actoplus Met®. On September 23, 2015, the District Court granted defendants’ motions to dismiss the indirect purchasers amended complaints with prejudice. The indirect purchasers filed a notice of appeal on October 22, 2015; however they have since abandoned and dismissed their appeal of the District Court’s dismissal of claims asserted against Mylan. The putative direct purchaser class filed an amended complaint on January 8, 2016. Defendants’ motion to dismiss was filed on January 28, 2016 and the briefing has been completed. The case has beenwas stayed pending the resolution of the indirect purchasers’ appeal against the defendants remaining in that case.
Shareholders Class Action
On June 11, 2015, City of Riviera Beach General Employees Retirement System and Doris Arnold (collectively, the “plaintiffs”) filed a purported class action complaint against Mylan and directors of Mylan Inc. (the “Directors”) in the Washington County, Pennsylvania, Court of Common Pleas (the “Pennsylvania Court”), on behalf of certain former shareholders of Mylan Inc. The complaint alleged both breach of fiduciary duty by the Directors and breach of contract by

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Mylanthat case. A decision was issued by the Second Circuit on February 8, 2017, reversing in part and affirming in part, the Directors, relating to certain public disclosures made in connection with the EPD Transaction and the organization of, and Call Option Agreement with, the Foundation. The plaintiffs asked the Pennsylvania Court to: find that the Directors breached their fiduciary duties and that Mylan and the Directors breached the purported contract, rescind the vote of Mylan Inc.’s former shareholders approving the EPD Transaction, award compensatory damages and award Plaintiffs their costs relatingDistrict Court’s decision as to the lawsuit. On June 22, 2015, Mylan andremaining defendants. Following this decision, the Directors removed the case to the U.S. District Court for the Western District of Pennsylvania (the “District Court”). The plaintiffsdirect purchasers filed an amended complaint in the District Court on July 10, 2015, that included the same basic causes of action and requested relief, dropped allegations against some of the Directors named in the original complaint and asserted the breach of contract claim not on behalf of a purported class of former shareholders of Mylan Inc. but on behalf of a purported subclass of such shareholders who held shares of Mylan continuously for a specified period following consummation of the EPD Transaction. On July 21, 2015, a second purported class action complaint against the same defendants, asserting the same basic claims and requesting the same basic relief on behalf of the same purported class and subclass, was filed by a different plaintiff in the District Court. On August 28, 2015, the District Court consolidated the three actions, and, on September 4, 2015, the plaintiffs in the consolidated action filed a consolidated amended complaint (the “Consolidated Amended Complaint”) against the same defendants, asserting the same basic claims and requesting the same basic relief on behalf of the same purported class and subclass, but asserting the breach of contract claim against only Mylan. On September 30, 2015, two of the plaintiffs in the consolidated action filed a motion for partial summary judgment, on the breach of contract claim against Mylan (the “Motion for Partial Summary Judgment”). On October 23, 2015, the District Court approved the voluntary dismissal of a third purported class action, commenced on August 28, 2015 against Mylan and the Directors, alleging federal securities and breach of contract claims against all defendants and breach of fiduciary duty claims against the Directors, all arising out of the same basic alleged facts and requesting the same basic reliefCourt has set a schedule for briefing on behalf of certain former shareholders of Mylan Inc. On November 25, 2015, the defendants filed a MotionSupplemental Motions to Dismiss the Consolidated Amended Complaint, and Mylan filed an Opposition to the Motion for Partial Summary Judgment and a Motion to Deny Summary Judgment. On December 21, 2015, the District Court consolidated the action with a fourth purported class action, commenced on November 24, 2015 by, among others, the plaintiff in the third action, against the same defendants, alleging only breach of contract arising out of the same basic alleged facts, and requesting the same basic relief on behalf of certain former shareholders of Mylan Inc. In consolidating the actions, the District Court ordered, among other things, that the Consolidated Amended Complaint would remain the operative complaint in the consolidated action and that the Motion for Partial Summary Judgment and Motion to Dismiss were not disturbed by the consolidation. A Report and Recommendation was issued by the Magistrate Judge on May 10, 2016, recommending to the District Court that the defendants’ Motion to Dismiss the plaintiffs’ Consolidated Amended Complaint be granted and that the case be dismissed with prejudice. The Magistrate Judge further recommended that the District Court deny the plaintiffs’ Motion for Partial Summary Judgment as moot. Briefing on the plaintiffs’ objections to the Report and Recommendation was completed on June 7, 2016. The District Court adopted the Report and Recommendation of the Magistrate Judge on August 12, 2016, dismissing the case with prejudice.Dismiss.
SEC Investigation
On September 10, 2015, Mylan N.V. received a subpoena from the SEC seeking documents with regard to certain related party matters. Mylan is fully cooperating with the SEC in its investigation, and we are unable to predict the outcome of this matter at this time.
EpiPen® Auto-Injector and Certain Congressional Matters
MDRP Classification of EpiPen® Auto-Injector and EpiPen Jr® Auto-Injector
In November 2014, the Company received a subpoena from the U.S. Department of Justice (“DOJ”) related to the classification of the EpiPen® Auto-Injector for purposes of the Medicaid Drug Rebate Program. The Company complied with various information requests received from the DOJ pursuant to the subpoena. The question in the underlying matter was whether EpiPen® Auto-Injector was properly classified with the Centers for MedicaidMedicare and MedicareMedicaid Services (“CMS”) as a non-innovator drug under the applicable definition in the Medicaid Rebate statute and subject to the formula that is used to calculate rebates to Medicaid for such drugs. EpiPen® Auto-Injector has been classified with CMS as a non-innovator drug since before Mylan acquired the product in 2007 based on longstanding written guidance from the federal government. Beginning in August 2016, questions regarding the pricing of the EpiPen® Auto-Injector significantly increased and the Company has received or has been the subject of additional inquiries, including with respect to the classification of EpiPen® Auto-Injector for purposes of the Medicaid Drug Rebate Program and certain other federal programs, from committees and members of Congress and from other federal and state governmental agencies.
Subsequent to these developments, on October 7, 2016, Mylan agreed to the terms of a $465 million settlement with the DOJ and other government agencies related to the classification of the EpiPen® Auto-Injector for purposes of the Medicaid Drug Rebate Program. The terms of the settlement do not provide for any finding of wrongdoing on the part of Mylan Inc. or

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any of its affiliated entities or personnel. The settlement terms provide for resolution of all potential Medicaid rebate liability claims by federal and state governments as to whether the product should have been classified as an innovator drug for CMSMedicaid Drug Rebate Program purposes, and subject to a higher rebate formula. EpiPen® Auto-Injector will begin being classified as an innovator drug on April 1, 2017. In connection with the settlement, Mylan expects to enter into a corporate integrity agreement with the Office of Inspector General of the Department of Health and Human Services. Mylan continues to work with the government to finalize the settlement. When the settlement is finalized, Mylan expects to classify the EpiPen® Auto-Injector as an innovator drug effective April 1, 2017. During the third quarter ofyear ended December 31, 2016, the Company recorded an accrual of $465 million related to the DOJ settlement which is included in other current liabilities in the Condensed Consolidated Balance Sheets.
SEC Document RequestRequest/Subpoena
On October 7, 2016, Mylan received a document request from the Division of Enforcement at the SEC seeking communications with the CMS and documents concerning Mylan products sold and related to the Medicaid Drug Rebate Program, and any related complaints. On November 15, 2016, Mylan intends toreceived a follow-up letter, modifying the initial document request, seeking information on and public disclosures regarding the settlement with the DOJ announced on October 7, 2016 and the classification of the EpiPen® Auto-Injector under the Medicaid Drug Rebate Program. On February 6, 2017, Mylan received a subpoena from the SEC in this matter, seeking additional documents. Mylan is fully cooperatecooperating with the SEC’s inquiry.
EpiPen® Auto-Injector FTC Request for Information
On November 18, 2016, Mylan received a request from the FTC Bureau of Competition seeking documents and information relating to its preliminary investigation into potential anticompetitive practices in the market for epinephrine auto-injectors. Mylan is fully cooperating with the FTC’s inquiry.
Federal Securities Litigation
Purported class action complaints were filed in October 2016 against Mylan N.V., Mylan Inc. and certain of their current and former directors and officers (collectively, for purposes of this paragraph, the “defendants”) in the United States

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District Court for the Southern District of New York on behalf of certain purchasers of securities of Mylan N.V. and/or Mylan Inc. on the NASDAQ. The complaints allegealleged that defendants made false or misleading statements and omissions of purportedly material fact, in violation of federal securities laws, in connection with disclosures relating to Mylan N.V. and Mylan Inc.’s classification of their EpiPen® Auto-Injector as a non-innovator drug for purposes of the Medicaid Drug Rebate Program. The complaints seeksought damages, as well as the plaintiffs’ fees and costs. On March 20, 2017, after the actions were consolidated, a consolidated amended complaint was filed, alleging substantially similar claims and seeking substantially similar relief, but adding allegations that defendants made false or misleading statements and omissions of purportedly material fact in connection with allegedly anticompetitive conduct with respect to EpiPen® Auto-Injector and certain generic drugs, and alleging violations of both federal securities laws (on behalf of a purported class of certain purchasers of securities of Mylan N.V. and/or Mylan Inc. on the NASDAQ) and Israeli securities laws (on behalf of a purported class of certain purchasers of securities of Mylan N.V. on the Tel Aviv Stock Exchange). Defendants’ response to the consolidated amended complaint is due May 30, 2017. We believe that the claims in these lawsuitsthe consolidated amended complaint are without merit and intend to defend against them vigorously.
EpiPen® Auto-Injector Israeli Securities Litigation
On October 13, 2016, a purported shareholder of Mylan N.V. filed a lawsuit, together with a motion to certify the lawsuit as a class action on behalf of certain Mylan N.V. shareholders on the Tel Aviv Stock Exchange, against Mylan N.V. and four of its directors and officers (collectively, for purposes of this paragraph, the “defendants”) in the Tel Aviv District Court (Economic Division). The plaintiff alleges that the defendants made false or misleading statements and omissions of purportedly material fact in Mylan N.V.’s reports to the Tel Aviv Stock Exchange regarding Mylan N.V.’s classification of its EpiPen® Auto-Injector for purposes of the Medicaid Drug Rebate Program, in violation of both U.S. and Israeli securities laws, the Israeli Companies Law and the Israeli Torts Ordinance. The plaintiff seeks damages, among other remedies. On January 19, 2017, the Court stayed this case until a final judgment is issued in the securities litigation currently pending in the United States District Court for the Southern District of New York. On April 30, 2017, another purported shareholder of Mylan N.V. filed a separate lawsuit, together with a motion to certify the lawsuit as a class action on behalf of certain Mylan N.V. shareholders on the Tel Aviv Stock Exchange, in the Tel Aviv District Court (Economic Division), alleging substantially similar claims and seeking substantially similar relief against the defendants and other directors and officers of Mylan N.V., but alleging also that this group of defendants made false or misleading statements and omissions of purportedly material fact in connection with allegedly anticompetitive conduct with respect to EpiPen® Auto-Injector and certain generic drugs, and alleging violations of both U.S. federal securities laws and Israeli law. Service of process has not been effected in the April 30, 2017 lawsuit. We believe that the claims in this lawsuitthese lawsuits are without merit and intend to defend against them vigorously.
EpiPen® Auto-Injector Civil Litigation
Beginning in August 2016, Mylan Specialty L.P. and other Mylan-affiliated entities have been named as defendants in certainthirteen putative class action lawsuitsactions relating to the pricing and/or marketing of the EpiPen® Auto-Injector. A Mylan officer and other non-Mylan affiliated companies also have been named as defendants in some of the class actions. These lawsuits were filed in the U.S. District Courts for the Northern District of California, Northern District of Illinois, District of Kansas, Eastern District of Michigan, Western District of Washington, District of New Jersey and the Western District of Pennsylvania, as well as the Hamilton County, Ohio Court of Common Pleas (later removed to the Southern District of Ohio). All but four of these lawsuits (one in Illinois, one in Washington and two in New Jersey) have either been dismissed or consolidated into a single putative class action pending in the U.S. District Court for the District of Kansas. The plaintiffs in these suitscases assert violations of various federal and state antitrust and consumer protection laws, the Racketeer Influenced and Corrupt Organizations Act (“RICO”), as well as common law claims, including claims for unjust enrichment, restitution, disgorgement and breach of the duty of good faith and fair dealing.claims. Plaintiffs’ claims include purported challenges to the prices charged for the EpiPen® Auto-Injector and/or the marketing of the product in packages containing two auto-injectors.auto-injectors, as well as allegedly anti-competitive conduct. Plaintiff in one of the putative class action lawsuits in New Jersey has filed a request with the Judicial Panel on Multidistrict Litigation to transfer all of the cases into a multidistrict litigation (“MDL”) proceeding in the District of New Jersey. We believe that the claims in these lawsuits are without merit and intend to defend against them vigorously.
On April 24, 2017, Sanofi-Aventis U.S., LLC (“Sanofi”) filed a lawsuit against Mylan Inc. and Mylan Specialty L.P. in the U.S. District Court for the District of New Jersey.  In this lawsuit, Sanofi alleges exclusive dealings and anti-competitive marketing practices in violation of the antitrust laws in connection with the sale and marketing of the EpiPen® Auto-Injector.  We believe that the claims in this lawsuit are without merit and intend to defend against them vigorously.

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EpiPen® Auto-Injector State AG Investigations
Beginning in August 2016, the Company and certain of its affiliated entities received subpoenas and informal requests from various state attorneys general seeking information and documents relating to the pricing and/or marketing of the EpiPen® Auto-Injector. The Company is fully cooperating with these inquiries.
EpiPen® Auto-Injector U.S. Congress/State Requests for Information and Documents
Beginning in August 2016, Mylan has also received several requests for information and documents from various Committees of the U.S. Congress and federal and state lawmakers concerning the marketing, distribution and sales of Mylan products. Mylan has cooperated and intends to engagecontinue cooperating with federal and state lawmakers as appropriate in response to their requests.

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The Company believes that it has strong defenses to current and future potential civil litigation, as well as governmental investigations and enforcement proceedings, althoughdiscussed in this “EpiPen® Auto-Injector and Certain Congressional Matters” section of this Note 19 Litigation. Although it is reasonably possible that the Company may incur additional losses from these matters, theany amount of which cannot be reasonably estimated at this time. In addition, the Company expects to incur additional legal and other professional service expenses associated with the EpiPen® Auto-Injector pricingsuch matters in future periods and will recognize these expenses as services are received. The Company believes that the ultimate amount paid for these services and claims could have a material effect on the Company's business, consolidated financial condition, results of operations, cash flows and/or ordinary share price in future periods.
Drug Pricing Matters
Department of Justice/Connecticut Subpoenas
On December 3, 2015, a subsidiary of Mylan N.V. received a subpoena from the Antitrust Division of the U.S. DOJ seeking information relating to the marketing, pricing, and sale of our generic Doxycycline products and any communications with competitors about such products.
On September 8, 2016, a subsidiary of Mylan N.V., as well as certain employees and a member of senior management, received subpoenas from the DOJ seeking additional information relating to the marketing, pricing and sale of our generic Cidofovir, Glipizide-metformin, Propranolol and Verapamil products and any communications with competitors about such products. Related search warrants also were executed. The Company is fully cooperating with the DOJ’s inquiry.
On December 21, 2015, the Company received a subpoena and interrogatories from the Connecticut Office of the Attorney General seeking information relating to the marketing, pricing and sale of certain of the Company’s generic products (including Doxycycline) and communications with competitors about such products. The Company is fully cooperating with Connecticut’s inquiry.
United States District Court for the Eastern District of Pennsylvania and Rhode IslandCivil Litigation
Beginning in March 2016, sixteenTwenty-two putative class action complaints have been filedare pending against Mylan Inc., Mylan Pharmaceuticals Inc. and other pharmaceutical manufacturers in a MDL in the United States District Court for the Eastern District of PennsylvaniaPennsylvania; plaintiff indirect purchasers, direct purchasers and oneindependent pharmacies generally allege anticompetitive conduct with respect to certain Doxycycline and Digoxin products. Mylan and its subsidiary believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

Twelve putative class action complaints have been filed in the District of Rhode Island by indirect purchasers against Mylan Inc., Mylan Pharmaceuticals Inc. and other pharmaceutical manufacturers alleging conspiracies to fix, raise, maintain and stabilize the prices of certain Doxycycline and Digoxin products and to allocate markets and customers for those products. In addition, three putative class action complaints have been filed in the Eastern District of Pennsylvania by direct purchasers against Mylan and other pharmaceutical manufacturers. The Judicial Panel on Multidistrict Litigation has established an MDL in the Eastern District of Pennsylvania, where the cases have been consolidated. Mylan and its subsidiary intend to deny liability and to defend these actions vigorously.
On September 21, 2016, a putative class action was filed in the United States District Court for the Eastern District of Pennsylvania byPennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Pravastatin products. These cases have been transferred to the MDL. Mylan and its subsidiary believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

Eight putative class action complaints have been filed against Mylan Inc., Mylan Pharmaceuticals Inc. and another pharmaceutical manufacturer in the United States District Court for the Eastern District of Pennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Divalproex products. These cases have been

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transferred to the MDL. Mylan and its subsidiary believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

Ten putative class action complaints have been filed against Mylan Pharmaceuticals Inc. and other pharmaceutical manufacturers alleging conspiraciesin the United States District Courts for the Southern District of New York and the Eastern District of Pennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to fix, maintain, and/or stabilizecertain Levothyroxine products. These cases have been transferred to the price of certain Pravastatin products.MDL. Mylan Pharmaceuticals Inc. believes that the claims in these lawsuits are without merit and intends to deny liability and to defend against them vigorously.

Ten putative class action complaints have been filed against Mylan Inc., Mylan Pharmaceuticals Inc., UDL Laboratories, Inc. and other pharmaceutical manufacturers in the United States District Courts for the Southern District of New York and the Eastern District of Pennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Propranolol products. The Defendants’ Motions to Dismiss the South District of New York cases was granted as to some state law claims but otherwise denied on April 6, 2017. These cases have been transferred to the MDL. Mylan and its subsidiaries believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

Eight putative class action complaints have been filed against Mylan Inc., Mylan Pharmaceuticals Inc., Mylan N.V. and another pharmaceutical manufacturer in the United States District Court for the District of Puerto Rico, the District of New Jersey and the Eastern District of Pennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Clomipramine products. These cases have been transferred to the MDL. Mylan and its subsidiaries believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

Four putative class action complaints have been filed against Mylan Inc., Mylan Pharmaceuticals Inc. and another pharmaceutical manufacturer in the U.S. District Court for the Eastern District of Pennsylvania; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Albuterol products. These cases have been transferred to the MDL. Mylan and its subsidiary believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

One putative class action complaint has been filed against Mylan Inc., Mylan Pharmaceuticals Inc. and another pharmaceutical manufacturer in the U.S. District Court for the Eastern District of Pennsylvania; plaintiff indirect purchaser generally alleges anticompetitive conduct with respect to certain Benazepril HCTZ products. This case has been transferred to the MDL. Mylan and its subsidiary believe that the claims in this lawsuit are without merit and intend to deny liability and to defend against them vigorously.

Four putative class action complaints have been filed against Mylan Inc., Mylan Pharmaceuticals Inc. and other pharmaceutical manufacturers in the U.S. District Court for the Eastern District of Pennsylvania and the U.S. District Court for the Southern District of New York; plaintiff indirect and direct purchasers generally allege anticompetitive conduct with respect to certain Amitriptyline products. These cases have been transferred to the MDL. Mylan and its subsidiary believe that the claims in these lawsuits are without merit and intend to deny liability and to defend against them vigorously.

A complaint was filed on January 31, 2017 by putative classes of direct and indirect purchasers against Mylan Pharmaceuticals Inc. and other pharmaceutical manufacturers in the United States District Court for the District of Connecticut. Plaintiffs generally allege anticompetitive conduct and RICO violations with respect to, among other things, certain Doxycycline products. This case has been transferred to the MDL. Mylan Pharmaceuticals Inc. believes that the claims in this lawsuit are without merit and intends to deny liability and to defend against them vigorously.

Attorney General Litigation
On December 14, 2016, attorneys general of twenty states filed a complaint in the United States District Court for the District of Connecticut against several generic pharmaceutical drug manufacturers, including Mylan, alleging anticompetitive conduct with respect to, among other things, Doxycycline Hyclate Delayed Release. On March 1, 2017, the complaint was amended to add the attorneys general of twenty additional states; the complaint alleges violation of federal and state antitrust laws, as well as violation of various states’ consumer protection laws. Certain of the Defendants have filed a request to transfer the case to the MDL. A decision on the request to transfer the case to the MDL remains pending. We believe that the claims in this lawsuit against Mylan are without merit and intend to defend against them vigorously.

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European Commission Proceedings
Perindopril
On or around July 8, 2009, the European Commission (the “Commission”) stated that it had initiated antitrust proceedings pursuant to Article 11(6) of Regulation No. 1/2003 and Article 2(1) of Regulation No. 773/2004 to explore possible infringement of Articles 81 and 82 EC and Articles 53 and 54 of the European Economic Area Agreement by Les Laboratoires Servier (“Servier”) as well as possible infringement of Article 81 EC by the Company’s Indian subsidiary, Mylan Laboratories Limited, and four other companies, each of which entered into agreements with Servier relating to the product Perindopril. On July 30, 2012, the Commission issued a Statement of Objections to Servier SAS, Servier Laboratories Limited, Les Laboratories Servier, Adir, Biogaran, Krka, d.d. Novo mesto, Lupin Limited, Mylan Laboratories Limited, Mylan, Niche Generics Limited, Teva UK Limited, Teva Pharmaceutical Industries Ltd., Teva Pharmaceuticals Europe B.V. and Unichem Laboratories Limited. Mylan Inc. and Mylan Laboratories Limited filed responses to the Statement of Objections. On July 9, 2014, the Commission issued a decision finding that Mylan Laboratories Limited and Mylan, as well as the companies noted above (with the exception of Adir, a subsidiary of Servier), had violated European Union competition rules and fined Mylan

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Laboratories Limited approximately €17.2 million, including approximately €8.0 million jointly and severally with Mylan Inc. The Company paid approximately $21.7 million related to this matter during the fourth quarter of 2014. In September 2014, the Company filed an appeal of the Commission’s decision to the General Court of the European Union. The briefing on appeal is complete and we are awaitingcomplete. A hearing on the schedulingappeal before the General Court of the hearing date.European Union has been scheduled for June 27, 2017.
Citalopram
On March 19, 2010, Mylan and Generics [U.K.] Limited, a wholly owned subsidiary of the Company, received notice that the Commission had opened proceedings against Lundbeck with respect to alleged unilateral practices and/or agreements related to Citalopram in the European Economic Area. On July 25, 2012 a Statement of Objections was issued to Lundbeck, Merck KGaA, Generics [U.K.] Limited, Arrow, Resolution Chemicals, Xelia Pharmaceuticals, Alpharma, A.L. Industrier and Ranbaxy. Generics [U.K.] Limited filed a response to the Statement of Objections and vigorously defended itself against allegations contained therein. On June 19, 2013, the Commission issued a decision finding that Generics [U.K.] Limited, as well as the companies noted above, had violated European Union competition rules and fined Generics [U.K.] Limited approximately €7.8 million, jointly and severally with Merck KGaA. Generics [U.K.] Limited has appealed the Commission’s decision to the General Court of the EU. Briefing on the appeal has been completed and a hearing took place on October 8, 2015. On September 8, 2016, the General Court dismissed all appeals against the European Commission’s decision. Mylan has untilfiled an appeal of the decision on November 18, 2016 to appeal the decision to European Court of Justice. The Company has accrued approximately $8.6$8.3 million and $9.8$8.2 million as of September 30, 2016March 31, 2017 and December 31, 2015,2016, respectively, related to this matter. It is reasonably possible that we will incur additional losses above the amount accrued but we cannot estimate a range of such reasonably possible losses at this time. There are no assurances, however, that settlements reached and/or adverse judgments received, if any, will not exceed amounts accrued. Generics [U.K.] Limited has also sought indemnification from Merck KGaA with respect to the €7.8 million portion of the fine for which Merck KGaA and Generics [U.K.] Limited were held jointly and severally liable. Merck KGaA has counterclaimed against Generics [U.K.] Limited seeking the same indemnification.
U.K. Competition and Markets Authority
Paroxetine
On August 12, 2011, Generics [U.K.] Limited received notice that the Office of Fair Trading (subsequently changed to the Competition and Markets Authority (the “CMA”)) was opening an investigation to explore the possible infringement of the Competition Act 1998 and Articles 101 and 102 of the Treaty on the Functioning of the European Union, with respect to alleged agreements related to Paroxetine. On April 19, 2013, a Statement of Objections was issued to Beecham Group plc, GlaxoSmithKline UK Limited, GlaxoSmithKline plc and SmithKline Beecham Limited (formerly, SmithKline Beecham plc) (together, “GlaxoSmithKline”), Generics [U.K.] Limited, Merck KGaA, Actavis UK Limited (formerly, Alpharma Limited), Xellia Pharmaceuticals ApS (formerly, Alpharma ApS) and Alpharma LLC (formerly, Zoetis Products LLC, Alpharma LLC, and Alpharma Inc.) (together, “Alpharma”), and Ivax LLC (formerly, Ivax Corporation) and Norton Healthcare Limited (which previously traded as Ivax Pharmaceuticals UK) (together, “Ivax”). Generics [U.K.] Limited filed a response to the Statement of Objections, defending itself against the allegations contained therein. The CMA issued a Supplementary Statement of Objections (“SSO”) to the above-referenced parties on October 21, 2014 and a hearing with regard to the SSO took place on December 19, 2014. The CMA issued a decision on February 12, 2016, finding that GlaxoSmithKline, Generics [U.K.] Limited, Merck KGaA and Alpharma, were liable for infringing EU and U.K. competition rules. With respect to Merck KGaA and

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Generics [U.K.] Limited, the CMA issued a penalty of approximately £5.8 million, for which Merck KGaA is liable for the entire amount; and of that amount Generics [U.K.] Limited is jointly and severally liable for approximately £2.7 million, which was accrued for at September 30, 2016.March 31, 2017. Generics [U.K.] Limited has appealed the decision. AThe hearing is scheduled to commence on February 27, 2017 before the Competition Appeals Tribunal.
Strides Arcolab Limited Settlement
At the acquisition date of Agila, the Company estimated and accrued approximately $20 million for contingent consideration related to certain escrow arrangements. On November 1, 2016, the Company and Strides agreedTribunal concluded on a settlement of substantially all outstanding regulatory, warranty and indemnity claims (the “Strides Settlement”). As a result of the settlement, the Company will have access to approximately $80 million of cash in the fourth quarter of 2016 which is currently contingently restricted. Approximately $110 million will be paid to either settle these pre-acquisition claims or be remitted to Strides. As such, the Company recorded approximately $90 million of expense in the third quarter of 2016. This amount is included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations for the three and nine months ended SeptemberMarch 30, 2016. Prior to the Strides Settlement, the maximum contingent consideration

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remaining was approximately $173 million and was related to the satisfaction of certain regulatory conditions, including potential regulatory remediation costs2017 and the resolution of certain pre-acquisition contingencies.parties are presently awaiting a decision.
Product Liability
The Company is involved in a number of product liability lawsuits and claims related to alleged personal injuries arising out of certain products manufactured and/or distributed by the Company, including but not limited to its Fentanyl Transdermal System, Phenytoin, Propoxyphene, Alendronate Sodium and Metoclopramide.Reglan. The Company believes that it has meritorious defenses to these lawsuits and claims and is vigorously defending itself with respect to those matters. From time to time, the Company has agreed to settle or otherwise resolve certain lawsuits and claims on terms and conditions that are in the best interests of the Company. The Company has accrued approximately $32.5$31.4 million and $9.5$31.5 million at September 30, 2016March 31, 2017 and December 31, 2015,2016, respectively. It is reasonably possible that we will incur additional losses and fees above the amount accrued but we cannot estimate a range of such reasonably possible losses or legal fees related to these claims at this time. There are no assurances, however, that settlements reached and/or adverse judgments received, if any, will not exceed amounts accrued.

Intellectual Property
In certain situations, the Company has used its business judgment to decide to market and sell products, notwithstanding the fact that allegations of patent infringement(s) or other potential third party rights have not been finally resolved by the courts. The risk involved in doing so can be substantial because the remedies available to the owner of a patent for infringement may include, a reasonable royalty on sales or damages measured by the profits lost by the patent owner. If there is a finding of willful infringement, damages may be increased up to three times. Moreover, because of the discount pricing typically involved with bioequivalent products, patented branded products generally realize a substantially higher profit margin than bioequivalent products. An adverse decision could have an adverse effect that is material to our business, financial condition, results of operations, cash flows and/or ordinary share price.

Other Litigation
The Company is involved in various other legal proceedings that are considered normal to its business, including but not limited to certain proceedings assumed as a result of the acquisition of the former Merck Generics business, Meda, Agila and the acquired EPD Business. The Company has approximately $10$20 million accrued related to these various other legal proceedings.proceedings at March 31, 2017. While it is not possible to predict the ultimate outcome of such other proceedings, the ultimate outcome of any such proceeding is not currently expected to be material to the Company’s business, financial condition, results of operations, cash flows and/or ordinary share price.


ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
The following discussion and analysis addresses material changes in the financial condition and results of operations of Mylan N.V. and subsidiaries for the periods presented. Unless context requires otherwise, the “Company”, “Mylan”, “our”, or “we” refer to Mylan N.V. and its subsidiaries. This discussion and analysis should be read in conjunction with the Consolidated Financial Statements, the related Notes to Consolidated Financial Statements and Management’s Discussion and Analysis of Financial Condition and Results of Operations included in Mylan N.V.’s Annual Report on Form 10-K for the year ended December 31, 2015,2016, as amended, the unaudited interim financial statements and related Notes included in Part I — ITEM 1 of this Quarterly Report on Form 10-Q (“Form 10-Q”) and our other Securities and Exchange Commission (the “SEC”) filings and public disclosures. The interim results of operations, for the three and nine months ended September 30, 2016comprehensive earnings and cash flows for the ninethree months ended September 30, 2016March 31, 2017 are not necessarily indicative of the results to be expected for the full fiscal year or any other future period.
This Form 10-Q contains “forward-looking statements.” These statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements may include, without limitation, statements about the acquisition of Meda AB (publ.) (“Meda”) by Mylan (the “Meda Transaction”), Mylan’s acquisition (the “EPD Transaction”) of Mylan Inc. and Abbott Laboratories’ non-U.S. developed markets specialty and branded generics business (the “EPD Business”), the potential benefits and synergies of the EPD Transaction and the Meda Transaction, future opportunities for Mylan and products, and any other statements regarding Mylan’s future operations, anticipated business levels, future earnings, planned activities, anticipated growth, market opportunities, strategies, competition, and other expectations and targets for future periods. These may often be identified by the use of words such as “will,” “may,” “could,” “should,” “would,” “project,” “believe,” “anticipate,” “expect,” “plan,” “estimate,” “forecast,” “potential,” “intend,” “continue,” “target” and variations of these words or comparable words. Because forward-looking statements inherently involve risks and uncertainties, actual future results may differ materially from those expressed or implied by such forward-looking statements. Factors that could cause or contribute to such differences include, but are not limited to: uncertainties related to the Meda Transaction; the possibility that Mylan will not be able to repurchase, repay or refinance Meda’s outstanding debt obligations on favorable terms or at all; the ability to meet expectations regarding the accounting and tax treatments of the EPD Transaction and the Meda Transaction; changes in relevant tax and other laws, including but not limited to changes in the U.S. tax code and healthcare and pharmaceutical laws and regulations in the U.S. and abroad; actions and decisions of healthcare and pharmaceutical regulators; the integration of the EPD Business and Meda being more difficult, time-consuming, or costly than expected; operating costs, customer loss, and business disruption (including, without limitation, difficulties in maintaining relationships with employees, customers, clients, or suppliers) being greater than expected following the EPD Transaction and the Meda Transaction; the retention of certain key employees of the EPD Business and Meda being difficult; the possibility that Mylan may be unable to achieve expected synergies and operating efficiencies in connection with the EPD Transaction and the Meda Transaction, and the December 2016 announced restructuring program in certain locations, within the expected time-frames or at all and to successfully integrate the EPD Business and Meda; with respect to the Medicaid Drug Rebate Program Settlement (as defined below), the inability or unwillingness on the part of any of the parties to agree to a finalfinalize the settlement, any legal or regulatory challenges to the settlement, and any failure by third parties to comply with their contractual obligations; expected or targeted future financial and operating performance and results; the capacity to bring new products to market, including but not limited to where Mylan uses its business judgment and decides to manufacture, market, and/or sell products, directly or through third parties, notwithstanding the fact that allegations of patent infringement(s) have not been finally resolved by the courts (i.e., an “at-risk launch”); any regulatory, legal, or other impediments to Mylan’s ability to bring new products, including but not limited to generic Advair, to market; success of clinical trials and Mylan’s ability to execute on new product opportunities;opportunities, including but not limited to generic Advair; any changes in or difficulties with our inventory of, and our ability to manufacture and distribute, the EpiPen® Auto-Injector and EpiPen Jr® Auto-Injector (collectively, “EpiPen® Auto-Injector”) to meet anticipated demand; the potential impact of any change in patient access to the EpiPen® Auto-Injector and the introduction of a generic version of the EpiPen® Auto-Injector; the scope, timing, and outcome of any ongoing legal proceedings, including government investigations, and the impact of any such proceedings on financial condition, results of operations, and/or cash flows; the ability to protect intellectual property and preserve intellectual property rights; the effect of any changes in customer and supplier relationships and customer purchasing patterns; the ability to attract and retain key personnel; changes in third-party relationships; the impact of competition; changes in the economic and financial conditions of the businesses of Mylan; the inherent challenges, risks, and costs in identifying, acquiring, and integrating complementary or strategic acquisitions of other companies, products, or assets and in achieving anticipated synergies; uncertainties and matters beyond the control of management; and inherent uncertainties involved in the estimates and judgments used in the preparation of financial statements, and the providing of estimates of financial measures, in accordance with accounting principles generally accepted in the United States of America (“U.S. GAAP”) and related standards or on an adjusted basis. For more detailed information on the risks and uncertainties associated with Mylan’s business activities, see the risks described in Mylan’s Annual Report on Form 10-K for the year ended December

December 31, 2015,2016, as amended Mylan’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2016, this Quarterly Report on Form 10-Q for the quarter ended September 30, 2016, and our other filings with the SEC. You can access Mylan’s filings with the SEC through the SEC website at www.sec.gov, and Mylan strongly encourages you to do so. Mylan undertakes no obligation to update any statements herein for revisions or changes after the filing date of this Form 10-Q.
Executive Overview
Mylan is a leading global pharmaceutical company, which develops, licenses, manufactures, markets and distributes generic, branded genericbrand name and specialty pharmaceuticals.over-the-counter (“OTC”) products in a variety of dosage forms and therapeutic categories. Mylan is committed to setting new standards in healthcare by creating better health for a better world, and our mission is to provide the world’s 7 billion people access to high quality medicine. To do so, we innovate to satisfy unmet needs; make reliability and service excellence a habit; do what’s right, not what’s easy; and impact the future through passionate global leadership.
Mylan offers one of the industry’s broadest product portfolios, including more than 2,7007,500 marketed products globally, to customers in more than 165 countries and territories. We operate a global, high quality vertically-integrated manufacturing platform which includes more than 50 manufacturing and research and development (“R&D”) facilities around the world and one of the world’s largest active pharmaceutical ingredient (“API”) operations. We also operate a strong and innovative research and development (“R&D&D”) network that has consistently delivered a robust product pipeline. Additionally, Mylan has a specialty business that is focused on respiratory and allergy therapies.pipeline, including complex products such as injectables.
Through the third quarter of 2016, Mylan had two segments, “Generics” and “Specialty.” Generics primarily develops, manufactures, sells and distributes generic or branded generic pharmaceutical products in tablet, capsule, injectable or transdermal patch form, as well as API. Our generic pharmaceutical business is conducted primarily in the United States (“U.S.”), Canada and Brazil (collectively, “North America”); Europe; and India, Australia, Japan and New Zealand as well as our export activity into emerging markets (collectively, “Rest of World”). Beginning in 2016, revenue from the Company’s Brazilian operation is included in the North America region. All prior period revenue from the Company’s Brazilian operations has been recast from the Rest of World region to the North America region to conform to the presentation for the current period. This change had no impact on Mylan’s segment reporting. Our API business is conducted through Mylan Laboratories Limited, which is included within Rest of World in our Generics segment. Specialty engages mainly in the development and sale of branded specialty injectable and nebulized products. We also report in Corporate/Other certain R&D expenses, general and administrative expenses, litigation settlements, amortization of intangible assets and certain purchase accounting items, impairment charges, if any, and other items not directly attributable to the segments.
Due to our acquisition of Meda on August 5, 2016 and the integration of our portfolio across our branded, generics and over-the-counter platforms in all of our regions, effectiveEffective October 1, 2016, the Company is expandingexpanded its reportable segments. The Company will report its resultssegments and now reports in three segments on a geographic basis as follows: (1) North America, (2) Europe and (3) Rest of World. This change in segment reporting will begin with the Company’s consolidated financial statements for the year ending December 31, 2016. Comparative segment financial information will behave been recast for prior periods to conform to this revised segment structure.
On August 25, 2016, the Company announced that it was immediately expanding already existing patient assistance programs for EpiPen® Auto-Injector. On August 29, 2016, the Company announced that its U.S. subsidiary will launch the first authorized generic to EpiPen® Auto-Injector. The Company intends to continue to market and distribute branded EpiPen® Auto-Injector.
Meda AB
On February 10, 2016, the Company issued an offer announcement under the Nasdaq Stockholm’s Takeover Rules and the Swedish Takeover Act (collectively, the “Swedish Takeover Rules”) setting forth a public offer to the shareholders of Meda AB (publ.) (“Meda”) to acquire all of the outstanding shares of Meda (the “Offer”), with an enterprise value, including the net debt of Meda, of approximately Swedish kronor (“SEK” or “kr”) 83.6 billion (based on a SEK/USD exchange rate of 8.4158) or $9.9 billion at announcement. On August 2, 2016, the Company announced that the Offer was accepted by Meda shareholders holding an aggregate of approximately 343 million shares, representing approximately 94% of the total number of outstanding Meda shares, as of July 29, 2016, and the Company declared the Offer unconditional. On August 5, 2016, settlement occurred with respect to the Meda shares duly tendered by July 29, 2016 and, as a result, Meda is now a controlled subsidiary of the Company. Pursuant to the terms of the Offer, each Meda shareholder that duly tendered Meda shares into the Offer received at settlement (1) in respect of 80% of the number of Meda shares tendered by such shareholder, 165kr in cash

per Meda share, and (2) in respect of the remaining 20% of the number of Meda shares tendered by such shareholder, 0.386 of the Company’s ordinary shares per Meda share (subject to treatment of fractional shares as described in the offer document published on June 16, 2016). The non-tendered shares will be acquired for cash through a compulsory acquisition proceeding, in accordance with the Swedish Companies Act (Sw. aktiebolagslagen (2005:551)), with advance title to such non-tendered shares expected to be acquired within six to twelve months of the acquisition date. The compulsory acquisition proceeding price will accrue interest as required by the Swedish Companies Act. Meda’s shares were delisted from the Nasdaq Stockholm exchange on August 23, 2016. On November 1, 2016, the Company made an offer to the remaining Meda shareholders to tender all their Meda shares for cash consideration of 161.31kr per Meda share (the “November Offer”) to provide such remaining shareholders with an opportunity to sell their shares in Meda to the Company in advance of the automatic acquisition of their shares for cash in connection with the compulsory acquisition proceeding. The acceptance period for the November Offer expires on November 23, 2016 and settlement is expected to occur on or around November 30, 2016. Meda shareholders who tender their shares in the November Offer will not have the right to withdraw their acceptances, and there are no conditions to the completion of the November Offer. Any Meda shareholders that do not accept the November Offer will automatically receive all-cash consideration plus statutory interest for their Meda shares as determined in the compulsory acquisition proceeding. The November Offer is not being made, nor will any tender of share be accepted from or on behalf of holders in, any jurisdiction in which the making of the November Offer or the acceptance of any tender of shares would contravene applicable laws or regulations or require any offer documents, filings or other measures. In connection with either the November Offer or the compulsory acquisition proceeding, it has been assumed that the fair value of the non-tendered shares would be approximately 161kr per share at settlement, and the shares will be purchased with all cash.
The total purchase price was approximately $6.92 billion, net of cash acquired, which includes cash consideration paid of approximately $5.3 billion, the issuance of approximately 26.4 million Mylan N.V. ordinary shares at a fair value of approximately $1.3 billion based on the closing price of the Company’s ordinary shares on August 5, 2016, as reported by the NASDAQ Global Select Stock Market (the “NASDAQ”) and an assumed liability of approximately $431.0 million related to the November Offer and the compulsory acquisition proceeding of the non-tendered Meda shares, which is classified as a current liability on the Condensed Consolidated Balance Sheet.
Refer to Note 4 Acquisitions and Other Transactions in “Item 1. Notes to Condensed Consolidated Financial Statements” for additional information regarding significant recent events, including other acquisitions and transactions.
Litigation Settlements and Other Contingencies, Net
On October 7, 2016, the Company agreed to the terms of a $465 million settlement with the U.S. Department of Justice and other government agencies related to the classification of the EpiPen® Auto-Injector for purposes of the Medicaid Drug Rebate Program (the “Medicaid Drug Rebate Program Settlement”). This amount is included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations for the three and nine months ended September 30, 2016.
On November 1, 2016, the Company and Strides agreed on a settlement of substantially all outstanding regulatory, warranty and indemnity claims (the “Strides Settlement”). As a result of the settlement, the Company will also have access to approximately $80 million of cash in the fourth quarter of 2016, which is currently contingently restricted. In addition,the Company announced restructuring programs in certain locations representing initial steps in a series of actions that are anticipated to further streamline our operations globally. The Company continues to develop the details of the cost reduction initiatives, including workforce actions and other potential restructuring activities beyond the programs already announced. During the three months ended March 31, 2017, the Company recorded approximately $90pre-tax charges of $23.1 million, of expense inwhich $11.5 million were non-cash asset impairment charges. The continued restructuring actions are expected to be implemented through fiscal year 2018. For the third quarterrestructuring activities that have been undertaken to date, the Company estimates that it will incur aggregate pre-tax charges ranging between $175.0 million and $225.0 million, inclusive of 2016. This amount is included in litigation settlementsthe 2016 and other contingencies, net inyear to date 2017 restructuring charges of $172.8 million. In addition, as a result of the Condensed Consolidated Statementsrestructuring activities that have been undertaken to date, management believes the potential annual savings will be between approximately $175.0 million and $225.0 million once fully implemented, with the majority of Operations forthese savings improving operating cash flow. At this time, the three and nine months ended September 30, 2016.
Referexpenses related to Note 18 Contingencies in “Item 1. Notes to Condensed Consolidated Financial Statements” forthe additional information regarding these two items.restructuring activities cannot be reasonably estimated.
Financial Summary
The tables below are a summary of the Company’s financial results for the three and nine months ended September 30, 2016March 31, 2017 compared to the prior year period:

 Three Months Ended    
 September 30,    
(In millions, except per share amounts)2016 2015 Change % Change
Total revenues$3,057.1
 $2,695.2
 $361.9
 13 %
Gross profit1,283.3
 1,315.3
 (32.0) (2)%
(Loss) earnings from operations(130.7) 601.1
 (731.8) (122)%
Net (loss) earnings attributable to Mylan N.V. ordinary shareholders(119.8) 428.6
 (548.4) (128)%
Diluted (loss) earnings per ordinary share attributable to Mylan N.V. ordinary shareholders$(0.23) $0.83
 $(1.06) (128)%
Earnings from operations decreased for the three months ended September 30, 2016 compared to the prior year period primarily due to the recognition of the Medicaid Drug Rebate Program Settlement and the Strides Settlement, both of which are included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations in the current quarter, as well as higher amortization expense and operating expenses related to acquisitions completed during 2016. These items were partially offset by an increase in total revenues and the tax benefit that the Company realized during the three months ended September 30, 2016.
 Nine Months Ended    
 September 30,    
(In millions, except per share amounts)2016 2015 Change % Change
Total revenues$7,809.1
 $6,938.6
 $870.5
 13 %
Gross profit3,362.0
 3,153.5
 208.5
 7 %
Earnings from operations385.8
 1,037.0
 (651.2) (63)%
Net earnings attributable to Mylan N.V. ordinary shareholders62.5
 653.0
 (590.5) (90)%
Diluted earnings per ordinary share attributable to Mylan N.V. ordinary shareholders$0.12
 $1.32
 $(1.20) (91)%
The decrease in earnings from operations for the nine months ended September 30, 2016 was primarily due to the Medicaid Drug Rebate Program Settlement and the Strides Settlement. In addition, diluted earnings per ordinary share attributable to Mylan N.V. ordinary shareholders for the nine months ended September 30, 2016 compared to the prior year period was also impacted by higher amortization expense and operating expenses related to acquisitions completed during 2016, losses related to the Company’s SEK denominated foreign currency contracts, the write off of financing fees related to the termination of the 2016 Bridge Credit Agreement (defined below) and a higher average share count due to the impact of the ordinary shares issued in the EPD Transaction. These items were partially offset by an increase in total revenues and the tax benefit that the Company realized during the nine months ended September 30, 2016.
 Three Months Ended    
 March 31,    
(In millions, except per share amounts)2017 2016 Change % Change
Total revenues$2,719.5
 $2,191.3
 $528.2
 24%
Gross profit1,085.0
 907.0
 178.0
 20%
Earnings from operations227.2
 105.6
 121.6
 115%
Net earnings66.4
 13.9
 52.5
 378%
Diluted earnings per ordinary share$0.12
 $0.03
 $0.09
 300%
A detailed discussion of the Company’s financial results can be found below in the section titled “Results of Operations.” As part of this discussion, we also report sales performance using the non-GAAP financial measure of “constant currency” third party net sales and total revenues. This measure provides information on the change in net sales assuming that foreign currency exchange rates had not changed between the prior and current period. The comparisons presented at constant currency rates reflect comparative local currency sales at the prior year’s foreign exchange rates. We routinely evaluate our third party net sales performance at constant currency so that sales results can be viewed without the impact of foreign currency exchange rates, thereby facilitating a period-to-period comparison of our operational activities, and believe that this

presentation also provides useful information to investors for the same reason. The following table compares third party net sales on an actual and constant currency basis for each reportable segment and the geographic regions within the Generics segment and consolidated total revenues on an actual and constant currency basis for the three and nine months ended September 30, 2016March 31, 2017 and 2015.2016.
More information about non-GAAP measures used by the Company as part of this discussion, including adjusted cost of sales, adjusted gross margins, adjusted earnings and adjusted EPS (all of which are defined below) can be found in “Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations - Results of Operations - Use of Non-GAAP Financial Measures.”


Results of Operations
Three Months Ended September 30, 2016March 31, 2017 Compared to Three Months Ended September 30, 2015March 31, 2016
 Three Months Ended
 September 30,
(In millions)2016 2015 % Change 
2016 Currency Impact (1)
 
2016 Constant Currency Revenues (2)
 Constant Currency % Change
Generics:           
Third party net sales           
North America (3)
$1,098.8
 $1,090.6
 1 % $(1.0) $1,097.8
 1 %
Europe (4)
842.0
 611.9
 38 % 7.9
 849.9
 39 %
Rest of World (3)
670.0
 535.9
 25 % (26.7) 643.3
 20 %
Total third party net sales (4)
2,610.8
 2,238.4
 17 % (19.8) 2,591.0
 16 %
            
Other third party revenues14.2
 11.5
 23 % 
 14.2
 23 %
Total third party revenues2,625.0
 2,249.9
 17 % (19.8) 2,605.2
 16 %
            
Intersegment sales (5)
27.4
 1.4
 NM
 
 27.4
 NM
Generics total revenues2,652.4
 2,251.3
 18 % (19.8) 2,632.6
 17 %
            
Specialty:           
Third party net sales418.7
 437.8
 (4)% 
 418.7
 (4)%
Other third party revenues13.4
 7.5
 79 % 
 13.4
 79 %
Total third party revenues432.1
 445.3
 (3)% 
 432.1
 (3)%
            
Intersegment sales (5)
7.2
 1.2
 NM
 
 7.2
 NM
Specialty total revenues439.3
 446.5
 (2)% 
 439.3
 (2)%
            
Elimination of intersegment sales (5)
(34.6) (2.6) NM
 
 (34.6) NM
Consolidated total revenues (4)
$3,057.1
 $2,695.2
 13 % $(19.8) $3,037.3
 13 %
 Three Months Ended
 March 31,
(In millions)2017 2016 % Change 
2017 Currency Impact (1)
 2017 Constant Currency Revenues 
Constant Currency % Change (2)
Third party net sales           
North America (3)
$1,214.9
 $1,157.5
 5% $(2.2) $1,212.7
 5%
Europe (3)
892.0
 584.3
 53% 24.3
 916.3
 57%
Rest of World (3)
580.5
 434.3
 34% (12.7) 567.8
 31%
Total third party net sales (3)
2,687.4
 2,176.1
 23% 9.4
 2,696.8
 24%
            
Other third party revenues32.1
 15.2
 111% 0.2
 32.3
 113%
Consolidated total revenues$2,719.5
 $2,191.3
 24% $9.6
 $2,729.1
 25%
____________
(1) 
Currency impact is shown as unfavorable (favorable).
(2) 
The constant currency revenuepercentage change is derived by translating third party net sales or revenues for the current period at prior year comparative period exchange rates.rates, and in doing so shows the percentage change from 2017 constant currency third party net sales or revenues to the corresponding amount in the prior year.
(3) 
Beginning in the first quarter ofEffective October 1, 2016, the Company reclassified sales fromexpanded its Brazilian operation fromreportable segments as follows: North America, Europe and Rest of World. As a result, the amounts previously reported under the Specialty segment have been recast to North America and amounts related to Brazil are included in Rest of World to North America. The amount reclassified for the three months ended September 30, 2015 was approximately $11.0 million.all periods presented.
(4)
For the three months ended September 30, 2015, adjusted third party net sales in Europe totaled $629.0 million, adjusted generics segment third party net sales totaled $2.26 billion and adjusted total revenues were $2.71 billion. Adjusted third party net sales in Europe, adjusted generics segment third party net sales, and adjusted total revenues are non-GAAP financial measures that are discussed further in the section titled Use of Non-GAAP Financial Measures.
(5)
The percentage changes in intersegment sales are considered not meaningful (or, “NM”) in terms of the Company’s total revenue as intersegment sales eliminate in consolidation.

Total Revenues
For the current quarter, Mylan reported total revenues of $3.062.72 billion, compared to $2.702.19 billion for the comparable prior year period, representing an increase of $361.9$528.2 million, or 13%24%. Total revenues include both net sales and other revenues from third parties. Third party net sales for the current quarter were $3.032.69 billion, compared to $2.682.18 billion for the comparable prior year period, representing an increase of $353.3$511.3 million, or 13%23%. Other third party revenues for the current quarter were $27.632.1 million, compared to $19.015.2 million for the comparable prior year period, an increase of $8.6$16.9 million. The increase in other third party revenues was principally the result of an increase in royalty income we are now receiving as a result of the acquisition of Meda.
The increase in total revenues includedwas the result of third party net sales growth in Generics of 17% as a result ofall segments. Contributing to this increase were net sales from the acquisitions of Meda and the Topicals Business, and to a lesser extent, net sales from products launched subsequent to October 1, 2015 (“new products”non-sterile, topicals-focused business (the “Topicals Business”), which combined totaledtogether totaling approximately $534.9$606.6 million. This increase was partially offset by a net decrease in net sales from new product introductions and existing products of approximately $218.6 million$85.8 million. The decrease from existing products was due to a combination of lower pricing and volumes in the current period. Mylan’s current quarter total revenues was unfavorably impacted by the effect of foreign currency translation. The favorableunfavorable impact of foreign currency translation on current period totalquarter revenues was approximately $19.8$10 million. As such, constant currency total revenues increased $537.8 million, or 25%.
From time to time, a limited number of our products may represent a significant portion of our net sales, gross profit and net earnings. Generally, this is due to the timing of new product introductions and the amount, if any, of additional competition in the market. Our top ten products in terms of sales, in the aggregate, represented approximately 30%19% and 33%26% of the Company’s total revenuesnet sales for the three months ended September 30,March 31, 2017 and 2016, and 2015, respectively.
Generics Segment
ForMylan offers one of the current quarter, Generics third party net sales were $2.61 billion, compared to $2.24 billion for the comparable prior year period, an increaseindustry’s broadest product portfolios, including generic, brand name and over-the-counter (“OTC”) products in a variety of $372.4 million, or 17%. In the Generics segment, foreign currency translation had a favorable impact on third party net sales of approximately $19.8 million, or 1%dosage forms and therapeutic categories. Generic products, particularly in the current quarter. As such, constant currency third party net sales increased by approximately $352.6 million, or 16% when compared to the prior year period. The graph below shows Generics third party net sales by region for the three months ended September 30, 2016 and 2015 and the increase period over period:
myl10q_20160xchart-09991.jpg
Third party net sales from North America increased by $8.2 million or 1% during the three months ended September 30, 2016 when compared to the prior year period. This increase was principally due to net sales from the acquisitions of Meda and the Topicals Business, and to a lesser extent, net sales from new product introductions as a result of leveraging our global platform, together totaling approximately $213.6 million. This increase was partially offset by lower volumes and pricing on existing products. The prior year period included the significant contribution of new products. The impact of foreign currency translation on current period third party net sales was insignificant within North America.
ProductsU.S., generally contribute most significantly to revenues and gross margins at the time of their launch, even more so in periods of market exclusivity, or in periods of limited generic competition. As such, the timing of new product introductions can have a significant

impact on the Company’s financial results. The entrance into the market of additional competition generally has a negative impact on the volume and pricing of the affected products. Additionally, pricing is often affected by factors outside of the Company’s control.

For branded products, the majority of the product’s commercial value is usually realized during the period in which the product has market exclusivity. In the U.S. and some other countries, when market exclusivity expires and generic versions of a product are approved and marketed, there can often be very substantial and rapid declines in the branded product’s sales. OTC products also participate in a competitive environment that includes both branded and private label products. In the OTC space, value is realized through innovation, access and consumer activation.
Third party net sales are derived from our three geographic reporting segments: North America, Europe and Rest of World. The graph below shows third party net sales by segment for the three months ended March 31, 2017 and 2016 and the increase period over period:
myl10q_20173xchart-51330.jpg
North America Segment
Third party net sales from North America increased by $57.4 million or 5% during the three months ended March 31, 2017 when compared to the prior year period. This increase was primarily due to net sales from the acquisitions of Meda and the Topicals Business which totaled approximately $182.1 million. These increases were partially offset by a net decrease in net sales from new product introductions and lower volume and pricing on existing products. As anticipated, the U.S. generics products experienced price erosion in the mid-single digits. Sales of the EpiPen® Auto-Injector declined in the current quarter as a result of increased competition and the impact of the launch of the authorized generic. The impact of foreign currency translation on current period third party net sales was less than 1% within North America.
Europe Segment
Third party net sales from Europe increased by $230.1307.7 million or 38%53% during the three months ended September 30, 2016March 31, 2017 when compared to the prior year period. The increase in third party net sales was primarily the result of net sales from the acquisition of Meda and towhich totaled approximately $337.8 million. This increase was partially offset by a lesser extent,net decrease in net sales from new product introductions totaling approximately $220.4 million in

the third quarter of 2016. Pricing and volumes were essentially flat in the third quarter of 2016 as a result of our diversified product portfolio.lower volume and pricing on existing products. The unfavorable impact of foreign currency translation on current period third party net sales was $7.9$24 million, or 1%4% within Europe. As such, constant currency third party net sales increased by approximately $238.0$332 million, or 39%57% when compared to the prior year period.
Third party net sales from Mylan’s business in France increased when compared to the prior year period primarily as a result of net sales from theThe acquisition of Meda significantly increased our operations and new product introductions,revenues throughout Europe, but particularly in France, Italy, Germany and Sweden. In France, we remain the generics market leader. In Italy, third party net sales increased when compared to the prior year period as a result of net sales from the acquisition of Meda.
Certain markets within Europe in which we do business have undergone government-imposed price reductions, and further government-imposed price reductions are expected in the future. Such measures, along with the tender systems discussed below, are likely to have a negative impact on sales and gross profit in these markets. However, government initiatives in certain markets that appear to favor generic products could help to mitigate this unfavorable effect by increasing rates of generic substitution and penetration.
Third party net sales from Rest of World increased by $134.1 million, or 25% during the three months ended September 30, 2016 when compared to the prior year period. This increase was primarily due to net sales from the acquisition of Meda principally in emerging markets, and to a lesser extent, net sales from new product introductions, together totaling approximately $101.1 million. In addition, net sales from existing products increased slightly, as higher volumes offset lower pricing throughout the region, including in our anti-retroviral (“ARV”) franchise. Sales within our ARV franchise progressively improved throughout the third quarter of 2016 as HIV tender volumes increased. Third party net sales from Rest of World were favorably impacted by the effect of foreign currency translation by approximately $26.7 million, or 5% during the three months ended September 30, 2016. As such, constant currency third party net sales increased by approximately $107.3 million, or 20%.
In addition to third party net sales, the Rest of World region also supplies finished dosage form (“FDF”) generic products and API to Mylan subsidiaries in conjunction with the Company’s vertical integration strategy. Intercompany sales recognized by Rest of World were approximately $249.0 million and $205.6 million in the three months ended September 30, 2016 and 2015, respectively. These intercompany sales eliminate within, and therefore are not included in Generics or consolidated third party net sales.
In Japan, third party net sales increased as a result of net sales from new products and higher volumes on existing products. These increases were partially offset by unfavorable pricing on existing products. In Australia, third party net sales increased primarily as a result of new product introductions, and to a lesser extent, net sales from the acquisition of Meda. As in Europe, both Australia and Japan have undergone government-imposed price reductions that have had, and could continue to have, a negative impact on sales and gross profit in these markets.
A number of markets in which we operate in Europe have implemented, or may implement, tender systems for generic pharmaceuticals in an effort to lower prices. Generally speaking, tender systems can have an unfavorable impact on sales and

profitability. Under such tender systems, manufacturers submit bids that establish prices for generic pharmaceutical products. Upon winning the tender, the winning company will receive preferential reimbursement for a period of time. The tender system often results in companies underbidding one another by proposing low pricing in order to win the tender. The loss of a tender by a third party to whom we supply API can also have a negative impact on our sales and profitability. Sales continue to be negatively affected by the impact of tender systems.

SpecialtyRest of World Segment
The graph below shows Specialty thirdThird party net sales for the three months ended September 30, 2016 and 2015 and the decrease period over period:
myl10q_20160xchart-11725.jpg
Specialty third party net sales decreasedfrom Rest of World increased by $19.1$146.2 million, or 4%34% during the three months ended September 30, 2016March 31, 2017 when compared to the prior year period. The decreaseThis increase was primarily driven by the acquisition of Meda which contributed net sales of approximately $86.7 million. In addition, net sales from existing products increased principally as a result of higher sales from our anti-retroviral (“ARV”) franchise. Throughout the segment, sales from new products and higher volumes on existing products more than offset lower unit volumes duepricing. Third party net sales from Rest of World were favorably impacted by the effect of foreign currency translation by approximately $13 million, or 3% during the three months ended March 31, 2017. As such, constant currency third party net sales increased by approximately $133 million, or 31%.
In addition to third party net sales, the Rest of World segment supplies finished dosage form (“FDF”) generic products and API, primarily from Mylan India, to Mylan subsidiaries in conjunction with the Company’s vertical integration strategy. Intercompany sales related to this strategy were approximately $89.8 million and $71.2 million in the three months ended March 31, 2017 and 2016, respectively. These intercompany sales eliminate within, and therefore are not included in the consolidated third party net sales.
In Australia, third party net sales increased primarily as a result of new product introductions, and to a lesser extent, the acquisition of Meda. Third party net sales in Japan were essentially flat when compared to the timing of wholesaler purchasesprior year period. As in Europe, both Australia and Japan have undergone government-imposed price reductions that have had, and could continue to have, a negative impact on sales and gross profit in these markets.
As a result of the EpiPen® Auto-Injectoracquisition of Meda, we have significantly expanded and strengthened our presence in anticipation ofemerging markets including China, Southeast Asia and the authorized generic launch.Middle East. These markets provide opportunities for future growth and expansion and are complemented by Mylan’s historical presence in India, Brazil and certain countries in Africa (including South Africa).
Cost of Sales and Gross Profit
Cost of sales increased from $1.38$1.28 billion for the three months ended September 30, 2015March 31, 2016 to $1.77$1.63 billion for the three months ended September 30, 2016,March 31, 2017, corresponding to the increase in sales. Cost of sales was primarily impacted by purchase accounting related amortization of acquired intangible assets, acquisition related costs and restructuring and other special items, which are described further in the section titled Use of Non-GAAP Financial Measures. Gross profit for the three months ended September 30, 2016March 31, 2017 was $1.28$1.09 billion and gross margins were 42%40%. For the three months ended September 30, 2015,March 31, 2016, gross profit was $1.32 billion$907.0 million and gross margins were 49%41%. Gross margins were negatively impacted in the current quarter by increased purchase accounting related items, primarily amortization expense as a result of the acquisitions of Meda and the Topicals Business andby approximately 365 basis points, lower gross profit from the significant contributionsales of existing products in North America, including the prior year period of new products.EpiPen® Auto-Injector, by approximately 250 basis points, partially offset by the contributions from the acquired businesses noted above. Adjusted gross margins were approximately 57%53% for the three months ended September 30, 2016,March 31, 2017, compared to approximately 58%54% for the three months ended September 30, 2015.March 31, 2016. For the quarter ended September 30, 2016, the acquisition of Meda and new product introductions each positively impactedMarch 31, 2017, adjusted gross margins were negatively impacted in the current quarter as a result of lower gross profit from the sales of existing products in North America, including the EpiPen® Auto-Injector, by 50approximately 150 basis points, respectively. These increases werepartially offset by the significant contribution incontributions from the prior year period of new products.acquired businesses noted above.

A reconciliation between cost of sales, as reported under U.S. GAAP, and adjusted cost of sales and adjusted gross margin for the three months ended September 30, 2016March 31, 2017 compared to the three months ended September 30, 2015March 31, 2016 is as follows:
 Three Months Ended
 September 30,
(In millions)2016 2015
U.S. GAAP cost of sales$1,773.8
 $1,379.9
Deduct:   
Purchase accounting related amortization(421.5) (215.4)
Acquisition related costs(8.5) (24.9)
Restructuring & other special items(21.7) (5.1)
Adjusted cost of sales$1,322.1
 $1,134.5
    
Adjusted gross profit (a)
$1,735.0
 $1,577.8
    
Adjusted gross margin (a)
57% 58%
 Three Months Ended
 March 31,
(In millions)2017 2016
U.S. GAAP cost of sales$1,634.5
 $1,284.3
Deduct:   
Purchase accounting amortization and other related items(343.3) (243.6)
Restructuring related costs(12.9) (1.4)
Acquisition related items(5.9) (18.5)
Other special items(7.1) (13.8)
Adjusted cost of sales$1,265.3
 $1,007.0
    
Adjusted gross profit (a)
$1,454.2
 $1,184.3
Adjusted gross margin (a)
53% 54%
____________
(a) 
Adjusted gross profit is calculated as total revenues (adjusted total revenues for 2015) less adjusted cost of sales. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues (adjusted total revenues for 2015).revenues.

Operating Expenses
Research & Development Expense
R&D expense for the three months ended September 30, 2016March 31, 2017 was $199.1217.5 million, compared to $174.8253.6 million for the comparable prior year period, an increasea decrease of $24.3$36.1 million. The increase is primarilydecrease was due to lower expenditures totaling approximately $47 million principally related to the Company’s respiratory and biologics programs due to the inclusiontiming of Meda andclinical activities when compared to the Topicals Business,prior year period. Partially offsetting these decreases was the impact of acquisitions which increased R&D expense by approximately $12$16 million in the current quarter.
In addition, in the first quarter of 2017, the Company entered into a joint development and marketing agreement for a respiratory product resulting in approximately $50 million in R&D expense also increased due to expenses of approximately $9.0 million inexpense. In the thirdfirst quarter of 2016, the Company made an upfront payment for $45 million related to the Company’s collaboration agreement entered into on January 8, 2016 with Momenta Pharmaceuticals, Inc. (“Momenta”). The remainder is driven by the continued development of our respiratory, insulin and biologics programs.
Selling, General & Administrative Expense
Selling, general and administrative expense (“SG&A”) for the current quarter was $656.9$631.3 million, compared to $537.1$549.3 million for the comparable prior year period, an increase of $119.8$82.0 million. The increase in SG&A is primarily due to the additional expense related to the acquisitions of Meda and the Topicals Business which increased SG&A by approximately $106.8$132.1 million in the current quarter. In addition, SG&A increased due to increased employeePartially offsetting this increase were lower acquisition related costs, including consulting and increased depreciation expense as a result of information technology related capital expenditures.legal costs, in the current quarter.
Litigation Settlements and Other Contingencies, Net
During the three months ended September 30, 2016March 31, 2017 and 2015,2016, the Company recorded a charge, net of $9.0 million and a gain, net of $558.0 million and $2.31.5 million, respectively. InDuring the current year period,three months ended March 31, 2017, the charge was primarilyCompany recorded a loss of $9.9 million to the fair value of contingent consideration related to the Medicaid Drug Rebate Program Settlement and the Strides Settlement.Jai Pharma Limited acquisition. In the prior year period, the chargegain was primarily related to the settlement of an anti-trustintellectual property matter.

Interest Expense
Interest expense for the three months ended September 30, 2016March 31, 2017 totaled $144.4138.2 million, compared to $95.170.3 million for the three months ended September 30, 2015,March 31, 2016, an increase of $49.3$67.9 million. The increase in the current quarter is primarily due to $59.3$74.6 million of interest expense related to the issuance of the senior notes in June of 2016 Senior Notes (as defined below) and approximately $17.7 millionthe Euro senior notes issued in December of interest related to borrowings acquired from Meda. Partially offsetting these increases2016. This increase was lower amortization of discounts as a result ofpartially offset by the repayment of the Company’s Cash Convertible1.800% Senior Notes due 2015 (the “Cash Convertible Notes”) in September 2015,2016 and the result1.350% Senior Notes due 2016 in June and November of the refinancing of certain debt instruments in 2015.2016, respectively.

Other Expense, Net
Other expense, net, was $50.2$17.4 million in the current quarter, compared to $50.9$16.3 million for the comparable prior year period. Other expense, net, includes losses from equity affiliates, foreign exchange gains and losses and interest and dividend income. Other expense, net was comprised of the following for the three months ended September 30,March 31, 2017 and 2016, and 2015, respectively:
 Three Months Ended September 30,
(In millions)2016 2015
Losses from equity affiliates, primarily clean energy investments$29.7
 $27.8
Foreign exchange losses (gains)27.8
 (17.2)
Write off of deferred financing fees
 11.1
Redemption premium on 2020 Senior Notes
 39.4
Write off of unamortized premium on 2020 Senior Notes
 (9.7)
Other gains, net(7.3) (0.5)
 $50.2
 $50.9
In the third quarter of 2016, foreign exchange losses of $27.8 million included $44.4 million of losses related to the Company’s SEK non-designated foreign currency contracts partially offset by foreign currency gains.
 Three Months Ended March 31,
(In millions)2017 2016
Losses from equity affiliates, primarily clean energy investments$33.2
 $30.9
Foreign exchange gains, net(10.3) (14.2)
Other gains, net(5.5) (0.4)
Other expense, net$17.4
 $16.3
Income Tax (Benefit) Provision
For the three months ended September 30, 2016,March 31, 2017, the Company recognized an income tax benefitprovision of $205.5$5.2 million, compared to an income tax provision of $26.5$5.1 million for the comparable prior year period. During the three months ended September 30, 2016, the Company received approvals from the relevant Indian regulatory authorities to legally merge its wholly owned subsidiary, Jai Pharma Limited, into Mylan Laboratories Limited. The merger resulted in the recognition of a deferredeffective tax asset of $150 million for the tax deductible goodwill in excess of the book goodwill with a corresponding benefit to income tax provisionrate was 7.3% and 26.8% for the three months ended September 30, 2016. In addition to the benefit recognized for the merger of the aforementioned entities, theMarch 31, 2017 and 2016, respectively. The effective tax rate for the three months ended September 30, 2016 versus the comparable prior quarter period was impacted by the Medicaid Drug Rebate Program Settlement.

Nine Months Ended September 30, 2016 Compared to Nine Months Ended September 30, 2015
 Nine Months Ended
 September 30,
(In millions)2016 2015 % Change 
2016 Currency Impact (1)
 
2016 Constant Currency Revenues (2)
 Constant Currency % Change
Generics:           
Third party net sales           
North America (3)
$3,028.6
 $2,894.1
 5% $10.9
 $3,039.5
 5%
Europe (4)
2,033.9
 1,589.2
 28% 10.2
 2,044.1
 29%
Rest of World (3)
1,613.9
 1,453.8
 11% (9.1) 1,604.8
 10%
Total third party net sales (4)
6,676.4
 5,937.1
 12% 12.0
 6,688.4
 13%
            
Other third party revenues33.0
 31.7
 4% 0.3
 33.3
 5%
Total third party revenues6,709.4
 5,968.8
 12% 12.3
 6,721.7
 13%
            
Intersegment sales (5)
29.5
 5.2
 NM
 0.3
 29.8
 NM
Generics total revenues6,738.9
 5,974.0
 13% 12.6
 6,751.5
 13%
            
Specialty:           
Third party net sales1,069.1
 950.7
 12% 
 1,069.1
 12%
Other third party revenues30.6
 19.1
 60% 
 30.6
 60%
Total third party revenues1,099.7
 969.8
 13% 
 1,099.7
 13%
            
Intersegment sales (5)
13.7
 5.8
 NM
 
 13.7
 NM
Specialty total revenues1,113.4
 975.6
 14% 
 1,113.4
 14%
            
Elimination of intersegment sales (5)
(43.2) (11.0) NM
 (0.3) (43.5) NM
Consolidated total revenues (4)
$7,809.1
 $6,938.6
 13% $12.3
 $7,821.4
 13%
____________
(1)
Currency impact is shown as unfavorable (favorable).
(2)
The constant currency revenue change is derived by translating third party net sales for the current period at prior year comparative period exchange rates.
(3)
Beginning in the first quarter of 2016, the Company reclassified sales from its Brazilian operation from Rest of World to North America. The amount reclassified for the nine months ended September 30, 2015 was approximately $32.3 million.
(4)
For the nine months ended September 30, 2015, adjusted third party net sales in Europe totaled $1.61 billion, adjusted generics segment third party net sales totaled $5.95 billion and adjusted total revenues were $6.96 billion. Adjusted third party net sales in Europe, adjusted generics segment third party net sales, and adjusted total revenues are non-GAAP financial measures that are discussed further in the section titled Use of Non-GAAP Financial Measures.
(5)
The percentage changes in intersegment sales are considered not meaningful (or, “NM”) in terms of the Company’s total revenue as intersegment sales eliminate in consolidation.
Total Revenues
For the nine months ended September 30, 2016, Mylan reported total revenues of $7.81 billion, compared to $6.94 billion for the comparable prior year period, representing an increase of $870.5 million, or 13%. Total revenues include both net sales and other revenues from third parties. Third party net sales for the nine months ended September 30, 2016 were $7.75

billion, compared to $6.89 billion for the comparable prior year period, representing an increase of $857.7 million, or 12%. Other third party revenues for the nine months ended September 30, 2016 were $63.6 million, compared to $50.8 million for the comparable prior year period, an increase of $12.8 million.
The increase in total revenues included third party net sales growth in Generics of 12% and Specialty of 12%. Contributing to this increase was net sales from the acquisitions of Meda and the Topicals Business and net sales from new product introductions, and to a lesser extent, the two additional months of net sales from the EPD Business (“incremental EPD Business sales”) in the Generics segment when compared to the nine months ended September 30, 2015, all of which combined totaled approximately $920.4 million. Net sales from existing products decreased approximately $67.9 million as a result of a decline in pricing of approximately $99.7 million, partially offset by an increase in volumes of approximately $31.8 million. Mylan’s total revenues were unfavorably impacted by the effect of foreign currency translation, primarily reflecting changes in the U.S. Dollar as compared to the currencies of Mylan’s subsidiaries in Canada, the European Union, India, and the United Kingdom, partially offset by the strengthening of the Japanese Yen. The unfavorable impact of foreign currency translation on current year total revenues was approximately $12.3 million resulting in an increase in constant currency total revenues of approximately $882.8 million, or 13%.
From time to time, a limited number of our products may represent a significant portion of our net sales, gross profit and net earnings. Generally, this is due to the timing of new product introductions and the amount, if any, of additional competition in the market. Our top ten products in terms of sales, in the aggregate, represented approximately 30% of the Company’s total revenues for the nine months ended September 30, 2016 and 2015, respectively.
Generics Segment
For the nine months ended September 30, 2016, Generics third party net sales were $6.68 billion, compared to $5.94 billion for the comparable prior year period, an increase of $739.3 million, or 12%. In the Generics segment, foreign currency translation had an unfavorable impact on third party net sales of approximately $12.0 million in the current year period. As such, constant currency third party net sales increased by approximately $751.3 million, or 13% when compared to the prior year period. The graph below shows Generics third party net sales by region for the nine months ended September 30, 2016 and 2015 and the increase period over period:
myl10q_20160xchart-10308.jpg
Third party net sales from North America increased by $134.5 million or 5% during the nine months ended September 30, 2016 when compared to the prior year period. This increase was principally due to net sales from the acquisitions of Meda, the Topicals Business, the incremental EPD Business sales, and to a lesser extent, net sales from new product introductions as a result of our global platform, together totaling approximately $312.5 million. This increase was partially offset by lower pricing on existing products while volumes on existing products increased slightly. The impact of foreign currency translation on the current period third party net sales was insignificant within North America.
Products generally contribute most significantly to revenues and gross margins at the time of their launch, even more so in periods of market exclusivity, or in periods of limited generic competition. As such, the timing of new product introductions can have a significant impact on the Company’s financial results. The entrance into the market of additional competition generally has a negative impact on the volume and pricing of the affected products. Additionally, pricing is often affected by factors outside of the Company’s control.
Third party net sales from Europe increased by $444.7 million or 28% during the nine months ended September 30, 2016 when compared to the prior year period. This increase was primarily the result of the acquisition of Meda, the incremental EPD Business sales, and to a lesser extent, net sales from new product introductions, together totaling approximately $408.5

million during the nine months ended September 30, 2016. In addition, there were higher volumes on existing products, while pricing was essentially flat as a result of our diversified product portfolio. The unfavorable impact of foreign currency translation on current period third party net sales was $10.2 million, or 1% within Europe. As such, constant currency third party net sales increased by approximately $454.9 million, or 29% when compared to the prior year period.
Third party net sales from Mylan’s business in France increased when compared to the prior year as a result of the acquisition of Meda and the incremental EPD Business sales, higher volumes and pricing on existing products and new product introductions. Our market share in France increased for the nine months ended September 30, 2016, and we remain the generics market leader. In Italy, third party net sales increased when compared to the prior year period as a result of the acquisition of Meda and the incremental EPD Business sales, and to a lesser extent, new product introductions, which was partially offset by lower sales of existing products.
Certain markets in Europe in which we do business have undergone government-imposed price reductions, and further government-imposed price reductions are expected in the future. Such measures, along with the tender systems discussed below, are likely to have a negative impact on sales and gross profit in these markets. However, government initiatives in certain markets that appear to favor generic products could help to mitigate this unfavorable effect by increasing rates of generic substitution and penetration.
Third party net sales from Rest of World increased by $160.1 million or 11% during the nine months ended September 30, 2016 when compared to the prior year period. This increase was primarily driven by the acquisition of Meda, the incremental EPD Business sales, and to a lesser extent, new product introductions across the region, together totaling $199.4 million, combined with higher sales volumes in Japan, India and emerging markets. These increases were partially offset by lower pricing in the region, including the ARV franchise. However, sales within our ARV franchise progressively grew throughout the first nine months of the year, and on a sequential basis third quarter sales increased over 30% from the second quarter of 2016. The favorable impact of foreign currency translation on current period third party net sales was $9.1 million, or 1% within Rest of World. As such, constant currency third party net sales increased by approximately $151.0 million, or 10%.
In addition to third party net sales, the Rest of World region also supplies FDF generic products and API to Mylan subsidiaries in conjunction with the Company’s vertical integration strategy. Intercompany sales recognized by Rest of World were approximately $684.1 million and $522.1 million in the nine months ended September 30, 2016 and 2015, respectively. These intercompany sales eliminate within, and therefore are not included in Generics or consolidated third party net sales.
In Japan, third party net sales increased as a result of the incremental EPD Business sales, higher volumes on existing products and net sales from new product introductions. In Australia, third party net sales increased as result of net sales from new product introductions, the incremental EPD Business sales, and to a lesser extent, the acquisition of Meda and higher volumes on existing products. Within these countries, net sales from existing products increased as higher volumes offset lower pricing. As in Europe, both Australia and Japan have undergone government-imposed price reductions that have had, and could continue to have, a negative impact on sales and gross profit in these markets.
A number of markets in which we operate have implemented, or may implement, tender systems for generic pharmaceuticals in an effort to lower prices. Generally speaking, tender systems can have an unfavorable impact on sales and profitability. Under such tender systems, manufacturers submit bids that establish prices for generic pharmaceutical products. Upon winning the tender, the winning company will receive preferential reimbursement for a period of time. The tender system often results in companies underbidding one another by proposing low pricing in order to win the tender. Additionally, the loss of a tender by a third party to whom we supply API can also have a negative impact on our sales and profitability. Sales continue to be negatively affected by the impact of tender systems.
Specialty Segment
The graph below shows Specialty third party net sales for the nine months ended September 30, 2016 and 2015 and the increase period over period:

myl10q_20160xchart-11932.jpg
Specialty third party net sales increased by $118.4 million or 12% during the nine months ended September 30, 2016 when compared to the prior year period. The increase was primarily the result of the realization of the benefits of customer contract negotiations over the last several quarters related to the EpiPen® Auto-Injector, and higher sales of the Perforomist® Inhalation Solution and ULTIVA®, partially offset by lower volumes across the segment.
Cost of Sales and Gross Profit
Cost of sales increased from $3.79 billion for the nine months ended September 30, 2015 to $4.45 billion for the nine months ended September 30, 2016, corresponding to the increase in sales. Cost of sales was primarily impacted by purchase accounting related amortization of acquired intangible assets, acquisition related costs and restructuring and other special items, which are described further in the section titled Use of Non-GAAP Financial Measures. In addition to the increase in net sales, the increase in cost of sales was also impacted by acquisition related amortization expense of Meda, the Topicals Business and Jai Pharma Limited as well as an additional two months of amortization expense related to the EPD Business as compared to the prior year period. Gross profit for the nine months ended September 30, 2016 was $3.36 billion and gross margins were 43%. For the nine months ended September 30, 2015, gross profit was $3.15 billion and gross margins were 45%. Gross margins were positively impacted in the current year by new product introductions and higher sales within Specialty which positively impacted gross margins by approximately 50 and 70 basis points, respectively. These increases were offset by the negative impact of increased purchase accounting related items, primarily amortization, as a result of the acquisitions of Meda and the Topicals Business, and the significant contribution in the prior year period of new products. Adjusted gross margins were approximately 56% for the nine months ended September 30, 2016, compared to approximately 55% for the nine months ended September 30, 2015. For the nine months ended September 30, 2016, the combined impact of acquisitions and new product introductions and higher sales within Specialty positively impacted adjusted gross margins by approximately 50 basis points and 30 basis points, respectively. These increases were partially offset by the significant contribution in the prior year period of new products.

A reconciliation between cost of sales, as reported under U.S. GAAP, and adjusted cost of sales and adjusted gross margin for the nine months ended September 30, 2016 compared to the nine months ended September 30, 2015 is as follows:
 Nine Months Ended
 September 30,
(In millions)2016 2015
U.S. GAAP cost of sales$4,447.1
 $3,785.1
Deduct:   
Purchase accounting related amortization(914.8) (598.3)
Acquisition related costs(39.8) (63.7)
Restructuring & other special items(47.9) (19.8)
Adjusted cost of sales$3,444.6
 $3,103.3
    
Adjusted gross profit (a)
$4,364.5
 $3,852.4
    
Adjusted gross margin (a)
56% 55%
____________
(a)
Adjusted gross profit is calculated as total revenues (adjusted total revenues for 2015) less adjusted cost of sales. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues (adjusted total revenues for 2015).

Operating Expenses
Research & Development Expense
R&D expense for the nine months ended September 30, 2016 was $632.2 million, compared to $512.9 million for the comparable prior year period, an increase of $119.3 million. During the nine months ended September 30, 2016, the Company made an upfront payment to Momenta for $45 million related to the Company’s collaboration agreement and incurred approximately $22.3 million of additional R&D expense related to the collaboration. The inclusion of Meda and the Topicals Business increased R&D expense by approximately $12 million and the additional two months of expense related to the EPD Business in the current year increased R&D expense by approximately $9 million. R&D expense also increased due to the continued development of our respiratory, insulin and biologics programs. During the nine months ended September 30, 2016, the Company incurred approximately $15 million of milestone payments related to the collaboration with Theravance Biopharma, Inc. (“Theravance Biopharma”). In the prior year period, the Company incurred a $15 million upfront licensing payment related to the collaboration with Theravance Biopharma.
Selling, General & Administrative Expense
SG&A for the nine months ended September 30, 2016 was $1.79 billion, compared to $1.58 billion for the comparable prior year period, an increase of $203.1 million. Factors contributing to the increase in SG&A include additional expense related to the acquisitions of Meda, the Topicals Business and the EPD Business which increased SG&A by approximately $175.4 million. In addition, the increase in SG&A is due to increased employee compensation expense as well as increased depreciation expense as a result of information technology related capital expenditures. These increases were partially offset by decreases in consulting and professional services expense of approximately $24.1 million and legal expense of approximately $27.0 million, primarily due to higher acquisition related costs incurred in the prior year period.
Litigation Settlements and Other Contingencies, Net
During the nine months ended September 30, 2016 and 2015, the Company recorded a charge, net of $556.4 million and $19.1 million, respectively. During the nine months ended September 30, 2016, the charge was primarily related to the Medicaid Drug Rebate Program Settlement and the Strides Settlement. In the prior year period, the charge was primarily related to the settlement of antitrust matters, partially offset by the settlement of patent infringement matters.

Interest Expense
Interest expense for the nine months ended September 30, 2016 totaled $305.0 million, compared to $268.5 million for the nine months ended September 30, 2015, an increase of $36.5 million. The increase in the current year is primarily due to approximately $73.2 million of interest related to the issuance of the June 2016 Senior Notes and approximately $17.7 million of interest related to borrowings acquired from Meda. Partially offsetting these increases was lower amortization of discounts as a result of the repayment of the Company’s Cash Convertible Notes in September 2015, and the result of the refinancing of certain debt instruments in 2015.
Other Expense, Net
Other expense, net, was $184.0 million for the nine months ended September 30, 2016, compared $71.4 million for the comparable prior year period. Other expense, net, includes losses from equity affiliates, foreign exchange gains and losses and interest and dividend income. Other expense, net was comprised of the following for the nine months ended September 30, 2016 and 2015, respectively:
 Nine Months Ended
 September 30,
(In millions)2016 2015
Losses from equity affiliates, primarily clean energy investments$85.5
 $77.5
Foreign exchange losses (gains)81.6
 (42.3)
Write off of deferred financing fees33.2
 11.0
Redemption premium on 2020 Senior Notes
 39.4
Write off of unamortized premium on 2020 Senior Notes
 (9.7)
Other gains, net(16.3) (4.5)
 $184.0
 $71.4
In the current year foreign exchange losses of approximately $81.6 million included $128.6 million of losses related to the Company’s SEK non-designated foreign currency contracts partially offset by foreign exchange gains.
Income Tax (Benefit) Provision
For the nine months ended September 30, 2016, the Company recognized an income tax benefit of $165.7 million, compared to an income tax provision of $44.0 million for the comparable prior year period. During the nine months ended September 30, 2016, the Company received approvals from the relevant Indian regulatory authorities to legally merge its wholly owned subsidiary, Jai Pharma Limited, into Mylan Laboratories Limited. The merger resulted in the recognition of a deferred tax asset of $150 million for the tax deductible goodwill in excess of the book goodwill with a corresponding benefit to income tax provision for the nine months ended September 30, 2016. In addition to the benefit recognized for the merger of the aforementioned entities, the effective tax rate for the nine months ended September 30, 2016March 31, 2017 versus the comparable prior year period was also impacted by the Medicaid Drug Rebate Program Settlement.changing mix of income earned in jurisdictions with differing tax rates, statutory releases of certain tax uncertainties and the revaluation of deferred tax assets and liabilities in countries that changed their statutory corporate tax rate.
Use of Non-GAAP Financial Measures
Whenever the Company uses non-GAAP financial measures, we provide a reconciliation of the non-GAAP financial measures to their most directly comparable U.S. GAAP financial measure. Investors and other readers are encouraged to review the related U.S. GAAP financial measures and the reconciliation of non-GAAP measures to their most directly comparable U.S. GAAP measure set forth below and should consider non-GAAP measures only as a supplement to, not as a substitute for or as a superior measure to, measures of financial performance prepared in accordance with U.S. GAAP. Additionally, since these are not measures determined in accordance with U.S. GAAP, non-GAAP financial measures have no standardized meaning across companies, or as prescribed by U.S. GAAP and, therefore, may not be comparable to the calculation of similar measures or measures with the same title used by other companies.
Management uses these measures internally for forecasting, budgeting, measuring its operating performance, and incentive-based awards. In addition, primarily due to acquisitions, we believe that an evaluation of our ongoing operations (and comparisons of our current operations with historical and future operations) would be difficult if the disclosure of our financial results was limited to financial measures prepared only in accordance with U.S. GAAP. We believe that non-GAAP financial

measures are useful supplemental information for our investors and when considered together with our U.S. GAAP financial measures and the reconciliation to the most directly comparable U.S. GAAP financial measure, provide a more complete understanding of the factors and trends affecting our operations. The financial performance of the Company is measured by senior management, in part, using adjusted metrics as described below, along with other performance metrics. Management’s annual incentive compensation is derived, in part, based on the adjusted EPS metric.
Adjusted Third Party Net Sales from Europe, Adjusted Generics Segment Third Party Net Sales, Adjusted Third Party Net Sales and Adjusted Total Revenues
The Company has provided the following non-GAAP financial measures: adjusted third party net sales from Europe, adjusted Generics segment third party net sales, adjusted third party net sales and adjusted total revenues, each of which excludes an acquisition related customer incentive in Europe from the most directly comparable U.S. GAAP financial measure for the three and nine months ended September 30, 2015.
 Three Months Ended Nine Months Ended
 September 30, September 30,
(In millions)2016 2015 2016 2015
U.S. GAAP third party net sales from Europe$842.0
 $611.9
 $2,033.9
 $1,589.2
Add:       
Acquisition related customer incentive
 17.1
 
 17.1
Adjusted third party net sales from Europe$842.0
 $629.0
 $2,033.9
 $1,606.3
U.S. GAAP Generics segment third party net sales$2,610.8
 $2,238.4
 $6,676.4
 $5,937.1
Add:       
Acquisition related customer incentive
 17.1
 
 17.1
Adjusted Generics segment third party net sales$2,610.8
 $2,255.5
 $6,676.4
 $5,954.2
U.S. GAAP third party net sales$3,029.5
 $2,676.2
 $7,745.5
 $6,887.8
Add:       
Acquisition related customer incentive
 17.1
 
 17.1
Adjusted third party net sales$3,029.5
 $2,693.3
 $7,745.5
 $6,904.9
U.S. GAAP total revenues$3,057.1
 $2,695.2
 $7,809.1
 $6,938.6
Add:       
Acquisition related customer incentive
 17.1
 
 17.1
Adjusted total revenues$3,057.1
 $2,712.3
 $7,809.1
 $6,955.7

Adjusted Cost of Sales and Adjusted Gross Margin
We use the non-GAAP financial measure “adjusted cost of sales” and the corresponding non-GAAP financial measure “adjusted gross margin.” The principal items excluded from adjusted cost of sales include restructuring, acquisition related and other special items and purchase accounting amortization and other related items, which are described in greater detail below.above.
Adjusted Earnings and Adjusted EPS
Adjusted net earnings attributable to Mylan N.V. (“adjusted earnings”) is a non-GAAP financial measure and provides an alternative view of performance used by management. Management believes that, primarily due to acquisition activity, an evaluation of the Company’s ongoing operations (and comparisons of its current operations with historical and future operations) would be difficult if the disclosure of its financial results were limited to financial measures prepared only in accordance with U.S. GAAP. AdjustedManagement believes that adjusted earnings and adjusted earnings per diluted share (“adjusted EPS”) are two of the most important internal financial metrics related to the ongoing operating performance of the Company, and management also believesare therefore useful to investors and that investors’their understanding of our performance is enhanced by these adjusted measures. Actual internal and forecasted operating results and annual budgets used by management include adjusted earnings and adjusted EPS.

The significant items excluded from adjusted cost of sales, adjusted earnings and adjusted EPS include:
Purchase Accounting Amortization and Other Related Items
The ongoing impact of certain amounts recorded in connection with acquisitions is excluded from adjusted cost of sales, adjusted earnings and adjusted EPS. These amounts include the amortization of intangible assets, and inventory step-up and intangible asset impairment charges, (includingincluding in-process research and development), accretion and the fair value adjustments related to contingent consideration.development.

Upfront and Milestone-Related R&D Expenses
These expenses and payments are excluded from adjusted earnings and adjusted EPS because they generally occur at irregular intervals and are not indicative of the Company’s ongoing operations. Also included in this adjustment are certain expenses related to the Company’s collaboration agreement with Momenta including certain milestone related costs. Such costs include payments related to Mylan’s future decisions, on a product by product basis, to continue with the development of such product in the collaboration after certain R&D work is performed. Related amounts are excluded from adjusted earnings as Mylan considers such payments as additional upfront buy-in payments for the products.

Accretion of Contingent Consideration Liability and Other Fair Value Adjustments
The impact of changes to the fair value of contingent consideration and accretion expense are excluded from adjusted earnings and adjusted EPS because they are not indicative of the Company’s ongoing operations due to the variability of the amounts and the lack of predictability as to the occurrence and/or timing and management believes it is helpful to understanding the underlying, ongoing operational performance of the business.
Restructuring, Acquisition Related and Other Special Items
Costs related to restructuring, acquisition and integration activities and other actions are excluded from adjusted cost of sales, adjusted earnings and adjusted EPS, as applicable. These amounts include items such as:
ExitCosts related to formal restructuring programs and actions, including costs associated with facilities to be closed or divested, including employee separation costs, impairment charges, accelerated depreciation, incremental manufacturing variances, equipment relocation costs and other restructuring related costs;
Certain acquisition related remediation and integration and planning costs, as well as other costs associated with acquisitions such as advisory and legal fees and certain financing related costs, and other business transformation and/or optimization initiatives, which are not part of a formal restructuring program, including employee separation and post-employment costs;

The pre-tax loss of the Company’s clean energy investments, whose activities qualify for income tax credits under Section 45 of the U.S. Internal Revenue Code of 1986, as amended (the “Code”); only included in adjusted earnings and adjusted EPS is the net tax effect of the entity’s activities; and
Certain costs to further develop and optimize our global enterprise resource planning systems, operations and supply chain.
The Company has undertaken restructurings and other optimization initiatives of differing types, scope and amount during the covered periods and, therefore, these charges should not be considered non-recurring; however, management excludes these amounts from adjusted earnings and adjusted EPS because it believes it is helpful to understanding the underlying, ongoing operational performance of the business.
Litigation Settlements, Net
Charges and gains related to legal matters, such as those discussed in the Notes to interim financial statements — Note 1819 ContingenciesLitigation are generally excluded from adjusted earnings and adjusted EPS. Normal, ongoing defense costs of the Company made in the normal course of our business are not excluded.
Reconciliation of Adjusted Earnings and Adjusted EPS
A reconciliation between net earnings attributable to Mylan N.V. ordinary shareholders and diluted (loss) earnings per share, attributable to Mylan N.V. ordinary shareholders, as reported under U.S. GAAP, and adjusted earnings and adjusted EPS for the periods shown follows:

Three Months Ended September 30, Nine Months Ended September 30,Three Months Ended March 31,
(In millions, except per share amounts)2016 2015 2016 20152017 2016
U.S. GAAP net (loss) earnings attributable to Mylan N.V. and U.S. GAAP diluted (loss) earnings per share$(119.8) $(0.23) $428.6
 $0.83
 $62.5
 $0.12
 $653.0
 $1.32
U.S. GAAP net earnings and U.S. GAAP diluted earnings per share$66.4
 $0.12
 $13.9
 $0.03
Purchase accounting related amortization (primarily included in cost of sales) (a)
427.1
   219.2
   931.8
   609.8
  349.2
   249.3
  
Litigation settlements, net (b)
468.0
   2.3
   466.4
   19.1
  (0.9)   (1.5)  
Interest expense (primarily related to clean energy investment financing)5.5
   11.5
   18.9
   39.9
  7.3
   5.7
  
Accretion of contingent consideration liability and other fair value adjustments (c)
100.4
   9.7
   120.7
   28.5
  17.7
   10.0
  
Clean energy investments pre-tax loss (d)(a)
23.8
   24.1
   69.4
   68.3
  22.3
   25.5
  
Financing related costs (included in other expense, net)
   40.8
   
   40.8
  
Acquisition related costs (primarily included in SG&A, other expense, net and interest expense) (e)
110.5
   92.3
   346.7
   243.7
  
Acquisition related customer incentive (included in third party net sales)
   17.1
   
   17.1
  
Restructuring and other special items included in:               
Acquisition related costs (primarily included in SG&A and cost of sales) (b)
31.3
   53.2
  
Restructuring related costs (c)
23.1
   9.8
  
Other special items included in:       
Cost of sales21.7
   5.1
   47.9
   19.8
  7.1
   13.8
  
Research and development expense (f)
22.2
   0.6
   98.7
   18.5
  
Research and development expense (d)
65.1
   66.1
  
Selling, general and administrative expense12.3
   8.6
   31.3
   41.3
  5.9
   6.8
  
Other expense, net(1.4)   (1.2)   1.3
   6.9
  6.1
   2.2
  
Tax effect of the above items and other income tax related items(343.9)   (124.9)   (490.5)   (289.5)  (100.8)   (68.5)  
Adjusted net earnings attributable to Mylan N.V. and adjusted diluted EPS$726.4
 $1.38
 $733.8
 $1.43
 $1,705.1
 $3.31
 $1,517.2
 $3.08
Adjusted net earnings and adjusted EPS$499.8
 $0.93
 $386.3
 $0.76
Weighted average diluted ordinary shares outstanding526.3
   514.0
   515.2
   493.2
  536.9
   509.6
  
____________
Significant items for the three months ended March 31, 2017 include the following:
(a) 
Includes amortization of the purchase accounting inventory fair value step-up for Meda, the Topicals Business and Jai Pharma Limited totaling approximately $56.1 million and $58.6 million for the three and nine months ended September 30, 2016. Includes amortization of the purchase accounting inventory fair value step-up for the EPD Business of approximately $35.4 million for the nine months ended September 30, 2015.
(b)
Includes $465 million related to the Medicaid Drug Rebate Program Settlement for the three and nine months ended September 30, 2016. This amount is included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations.
(c)
Includes approximately $90 million related to the Strides Settlement for the three and nine months ended September 30, 2016. This amount is included in litigation settlements and other contingencies, net in the Condensed Consolidated Statements of Operations.
(d)
Adjustment represents exclusion of the pre-tax loss related to Mylan's clean energy investments and related financing, excluding interest expense, the activities of which qualify for income tax credits under Section 45 of the Code. The amount is included in other expense, net in the Condensed Consolidated Statements of Operations.
(e) (b) 
Acquisition related costs primarily relate to ongoing acquisition and integration activities, including ongoing activities. Such costs included in other expense, net is approximately $44.4 million and $128.6 million of losses related to the Company's SEK non-designated foreign currency contracts for the three and nine months ended September 30, 2016, respectively. Included in SG&A for the three and nine months ended September 30, 2016March 31, 2017 is approximately $39.7$24.1 million, and $102.4 million, respectively, primarily related to consulting, professional and legal costs. Included
(c)
Refer to Note 17Restructuring included in interest expense, net forItem 1 in this Form 10-Q. Of the threetotal amount, approximately $12.9 million is included in cost of sales, $1.3 million is included in R&D and nine months ended September 30, 2016$8.9 million is approximately $19.7 million and $33.6 million of interest expense, respectively, related to the issuance of June 2016 Senior Notes for the period prior to the completion date of the Offer.included in SG&A.

(f)(d)
R&D expense includes an upfront expense of approximately $50 million related to a $45joint development and marketing agreement for a respiratory product, $5.8 million upfront paymentrelated to Momenta collaboration expense and $15 million of milestone payments to Theravance Biopharma for the nine months ended September 30, 2016. In addition, included in this amount for the three and nine months ended September 30, 2016 is approximately $9.0 million and $22.3 million, respectively, of R&D expense incurred related to the Company’s collaboration with Momenta.other similar smaller agreements.

Liquidity and Capital Resources
Our primary source of liquidity is cash provided by operations, which was $1.70 billion$452.9 million for the ninethree months ended September 30, 2016.March 31, 2017. We believe that cash provided by operating activities and available liquidity will continue to allow us to meet our needs for working capital, capital expenditures and interest and principal payments on debt obligations. Nevertheless, our ability to satisfy our working capital requirements and debt service obligations, or fund planned capital expenditures, will substantially depend upon our future operating performance (which will be affected by prevailing economic conditions), and financial, business and other factors, some of which are beyond our control.
Operating Activities
myl10q_20160xchart-09491.jpg
Net cash provided by operating activities increased by $341.2$372.4 million to $1.70 billion$452.9 million for the ninethree months ended September 30, 2016,March 31, 2017, as compared to net cash provided by operating activities of $1.36 billion$80.5 million for the ninethree months ended September 30, 2015. March 31, 2016. Cash provided by operating activities is derived by net earnings adjusted for non-cash operating items, gains and losses attributed to investing and financing activities and changes in operating assets and liabilities resulting from timing differences between the receipts and payments of cash, including changes in cash primarily reflecting the timing of cash collections from customers, payments to vendors and employees and tax payments in the ordinary course of business.
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The net increase in cash provided by operating activities was principally due to the following:

an increase in non-cash expenses of $1.09 billion includingnet earnings for the three months ended March 31, 2017 increased depreciation and amortization$52.5 million when compared to the prior year period, principally as a result of recent acquisitions of approximately $355.0 million, $465.0 million related to the Medicaid Drug Rebate Program Settlement, $90 million related to the Strides Settlement, the write off of certain financing fees and a number of other charges including the accretion of contingent consideration and increased losses in equity method investments;
a netan increase in the amount ofearnings from operations. Other significant factors impacting cash provided by changes in accounts receivable, including estimated sales allowances of $237.6 million, reflecting the timing of sales, cash collections and disbursements related to sales allowances; and
a net decreaseoperating activities in the amount of cash used in changes in income taxes payable of $229.8 million as a result of a lower amount of estimated tax payments made duringcurrent year include the current year.following:
an increase in non-cash expenses of $140.8 million, principally a result of increased depreciation and amortization as a result of recent acquisitions of approximately $118.4 million;
a net increase in the amount of cash provided by changes in accounts receivable, including estimated sales allowances, of $203.2 million, reflecting the timing of sales, cash collections and customer credits issued related to sales allowances;
a net decrease of $117.2 million in the amount of cash used through changes in inventory balances; and
an net increase in the amount of cash provided by changes in other operating assets and liabilities of $134.5 million, primarily due to higher amounts of accrued interest as a result of the long-term debt issuances during 2016 and the timing of interest payments related to those debt instruments.
These items were partially offset by the following:
a decrease in net earnings of $590.6 million, including a $294.4 million increase in the benefit for deferred income taxes; and
a net decrease in the amount of cash provided byused through changes in trade accounts payable of $287.5$185.5 million as a result of the timing of cash payments.payments; and
a net increase in the amount of cash used through changes in income taxes of $90.3 million as a result of the level and timing of estimated tax payments made during the current period.

Investing Activities
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Cash used in investing activities was $7.08 billion$164.1 million for the ninethree months ended September 30, 2016,March 31, 2017, as compared to $639.3$160.0 million for the ninethree months ended September 30, 2015,March 31, 2016, a net increase of $6.44 billion. The net increase in cash used$4.1 million.
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In 2017, significant items in investing activities was principally the result ofincluded the following:
an increase in net cash paid for acquisitions, of $6.15 billion which relatesnet totaling approximately $71.6 million related to the Company’s acquisitions of Meda and the Topicals Business;
an unconditional deferred payment of $308 million relating to Meda’s acquisition of Rottapharm S.p.A paid in the third quarter of 2016 as a result of the acquisition of Meda;the remaining non-tendered shares of Meda in the compulsory acquisition proceeding;
a $128.6 million settlement of the Company’s non-designated foreign exchange forwardpayments for product rights and option contracts used to economically hedge the foreign currency exposure associated with theother, net totaled approximately $77.9 million, which included a payment of $50 million related to the Swedish krona-denominated cash portionacquisition of intellectual property rights for the purchase priceCold-EEZE® brand cold remedy line;
proceeds from the sale of Meda;
certain European assets for approximately $31.1 million;
an increasea decrease in restricted cash of $76.4 million. In$12.7 million in the current year, restricted cash increased approximately $50 millionquarter due to amounts released from escrow for the payment of certain claims related to amounts deposited in escrow for potentialthe Agila contingent consideration payments in connection with the acquisition of the Topicals Business;consideration; and
an increase in capital expenditures, primarily for equipment and facilities, which totaled approximately $239.5 million in the current period, compared to $207.3 million in the comparable prior year period.$58.4 million. While there can be no assurance that current expectations will be realized, capital expenditures for the 20162017 calendar year are expected to be approximately $400 million to $450$500 million.
TheseIn 2016, significant items were partially offset byin investing activities included the following:
a decrease in payments for product rights and other, investing activities, net totaled approximately $105.6 million which totaled $196.3 million for the nine months ended September 30, 2016, as compared to $428.2 million in the prior year period. In the current year, the Company paid $57.9 million to acquireincluded a marketed pharmaceutical product andpayment of $90 million related to acquirethe acquisition of certain European intellectual property rights and marketing authorizations, which was accruedauthorizations; and
capital expenditures, primarily for at December 31, 2015. The prior year payments were the result of the acquisition of certain commercialization rights in the U.S.equipment and other countries; and
a decrease in the purchase of marketable securities, whichfacilities, totaled $22.8approximately $51.8 million during the nine months ended September 30, 2016, as compared to $59.1 million in the prior year period. This change is primarily attributable to the Company’s investment in Theravance Biopharma’s common stock in the prior year..

Financing Activities
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Cash provided by financing activities was $5.39 billion for the nine months ended September 30, 2016, compared to cash used in financing activities of $318.7was $575.7 million for the ninethree months ended September 30, 2015, a net increase of $5.71 billion. The net increase inMarch 31, 2017, compared to cash provided by financing activities was principallyof $30.5 million for the resultthree months ended March 31, 2016, a net decrease of $606.2 million.

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In 2017, significant items in financing activities included the following:
an increase in proceeds from long-term debtthe Company voluntarily prepaid $550 million of $4.1 billion which was attributable to the Company’s issuance of $1.00 billion aggregate principal amount of 2.500% Senior Notes due 2019, $2.25 billion aggregate principal amount of 3.150% Senior Notes due 2021, $2.25 billion aggregate principal amount of 3.950% Senior Notes due 2026,the 2016 Term Loans: and $1.00 billion aggregate principal amount of 5.250% Senior Notes due 2046 (collectively, the “June 2016 Senior Notes”) in the second quarter of 2016 in anticipation of the completion of the acquisition of Meda. In the prior year period,
the Company received proceedshad net repayments of approximately $2.4 billion under various financings;
a decrease in payments of long-term debt, which totaled $1.07 billion for the nine months ended September 30, 2016, as compared to $4.33 billion for the nine months ended September 30, 2015. In the current year, the Company paid the principal amount of $500.0 million on the 1.800% Senior Notes due 2016 which matured on June 24, 2016 and repaid approximately $567 million of Meda’s bank loans. In the prior year, the Company paid $2.54 billion in connection with the conversion of the Cash Convertible Notes on September 15, 2015 and paid $1.08 billion in connection with the redemption of the 7.875% Senior Notes due 2020 (the “2020 Senior Notes”); and
an increase in the change in short-term borrowings of $378.3$17.6 million.
In 2016, significant items in financing activities included the prior year period, following:
the Company decreased thehad net short-term borrowings under the accounts receivable securitization facility (the “Receivables Facility”) by approximately $325 million, net.
These items wereof $65.1 million; partially offset by the following:
a decrease in proceeds from the cash convertible note hedgepayments of financing fees which totaled $1.97 billion in$31.6 million primarily related to a bridge credit agreement related to the prior year as the cash convertible note hedge settled in the third quarter of 2015 in conjunction with the maturity and full redemption of the Cash Convertible Notes; and

a decrease in proceeds from the exercise of stock options which totaled $11.1 million in the current year, as compared to $92.8 million in the prior year period.

Meda acquisition.
Capital Resources
Our cash and cash equivalents at our non-U.S. operations totaled $1.19 billion$700.9 million at September 30, 2016. TheseMarch 31, 2017. The majority of these funds are availablerepresented earnings considered to purchasebe permanently reinvested to support the non-tendered Meda shares through the November Offer and compulsory acquisition proceeding.growth strategies of our non-U.S. subsidiaries. The Company anticipates having sufficient U.S. liquidity, including existing borrowing capacity under the 2016 Revolving Facility and the Receivables Facility combined with cash to be generated from operations, to fund foreseeable U.S. cash needs without requiring the repatriation of non-U.S. cash. If these funds are ultimately needed for the Company’s operations in the U.S., the Company may be required to accrue and pay U.S. taxes to repatriate these funds. If funds are needed from the Company’s subsidiaries that do not have an ultimate U.S. parent, the Company will generally not be required to accrue and pay taxes to repatriate these funds because its foreign parent would not be subject to tax on receipt of these distributions.

Meda Borrowings
Upon settlement of the Offer on August 5, 2016, Meda became a controlled subsidiary of Mylan. Meda is party to certain debt obligations, all of which remained outstanding following the settlement of the Offer. During the three months ended September 30, 2016, the Company repaid approximately $567 million of Meda’s bank loans. Meda’s outstanding debt obligations and committed bank facilities contained change of control provisions that were triggered upon settlement of the Offer. Meda’s debt financing includes approximately 16.7kr billion of borrowings under a syndicated bank facility of 25kr billion with nine Swedish and foreign banks. This financing is augmented with borrowings via a Swedish MTN program with an upper limit of 7kr billion, a Swedish commercial paper program with an upper limit of 4kr billion and a bilateral bank loan of 2kr billion.
The settlement of the Offer constituted a change of control under the Facilities Agreement, dated as of December 17, 2014 (as amended on October 29, 2015, the “Facilities Agreement”), among Meda, as borrower, the lenders party thereto (the “Lenders”) and Danske Bank A/S, as agent (“Danske”). As of September 30, 2016, there was $1.94 billion aggregate principal amount of loans outstanding under the Facilities Agreement. On August 30, 2016, Meda entered into the Amendment and Waiver Letter (the “Amendment”) to the Facilities Agreement, between Meda, as borrower, and Danske Bank A/S, as agent on behalf of the Lenders. The Amendment provides that (i) the lenders under the Facilities Agreement waive any put rights arising in connection with the Company’s acquisition of a majority of the issued share capital in Meda or any action taken in connection therewith; (ii) the termination date in respect of each of the loans and commitments under the Facilities Agreement will be August 30, 2017; and (iii) a change of control will occur under the Facilities Agreement if (a) the Company fails to, directly or indirectly, own all or substantially all of the issued share capital or votes in Meda or (b) any person (other than Stichting Preferred Shares Mylan) acquires more than 50% of the issued share capital or votes in the Company. Of the total facility amount of 25kr billion, the Company has available approximately 7.9kraccess to $2.0 billion ($925.1 million) of uncommitted borrowings at September 30, 2016.
The settlement of the Offer constituted a change of control under the terms of the notes issued by Meda under its MTN program. In accordance with the terms of the notes, Meda notified the noteholders of the occurrence of the change of control on August 5, 2016. As of September 30, 2016, there was $157.5 million aggregate principal amount of notes outstanding under the MTN program. As a result of such change of control, each noteholder had an individual right (a “put right”) to demand early redemption of the notes at their principal amount, together with accrued interest up to and including the date of redemption. The date of redemption for the notes of the noteholders that chose to exercise their put rights was November 3, 2016 and approximately $2.0 million was paid on that date.
The settlement of the Offer constituted a Change of Control (as defined in the Loan Agreement referred to below) under the Loan Agreement, dated as of September 17, 2014 (the “Loan Agreement”), between Meda, as borrower, and AB Svensk Exportkredit (publ), as lender (“Svensk Exportkredit”). As of September 30, 2016, there was $233.3 million aggregate principal amount of loans outstanding under the Loan Agreement. In accordance with the terms of the Loan Agreement, Meda notified Svensk Exportkredit of the Change of Control. No agreement to amend the terms of the Loan Agreement was reached within 30 days of Svensk Exportkredit’s receipt of notice from Meda of the Change of Control. Svensk Exportkredit may cancel its commitment and demand repayment of the loans under the Loan Agreement by notice to Meda, with repayment to be made not less than 30 days after such notice to Meda. The loans under the Loan Agreement will be repaid in accordance with the terms thereof.
The Facilities Agreement contains customary affirmative covenants, including among others, covenants pertaining to the delivery of financial statements, notices of default and certain material events, maintenance of authorizations, property, and insurance and compliance with laws, as well as customary negative covenants, including limitations on the incurrence of subsidiary indebtedness, disposals, loans and guarantees, liens, mergers and certain other corporate reconstructions, acquisitions and changes in Meda’s lines of business. Pursuant to the Facilities Agreement, Meda must deliver to Danske (i) within 60 days after the end of each consecutive three month period of its financial years, its unaudited consolidated financial statements for such three month period and (ii) within 120 days after the end of each of its financial years, its audited consolidated financial statements for such financial year. The Facilities Agreement contains financial covenants limited to (i) a maximum senior net debt to EBITDA ratio and (ii) a minimum EBITDA interest coverage ratio.
The MTN program contains covenants that, among other things, restrict Meda's ability and the ability of certain of Meda's subsidiaries to substantially change the general nature of its business; create liens to secure debt securities or other publicly traded debt; or sell or dispose of Meda's assets to the extent such sales or disposition could jeopardize Meda’s ability to fulfill its obligations under the MTN program; and require Meda to maintain the listing of the loans under the MTN program on

Nasdaq Stockholm. As long as the loans under the MTN program are listed on Nasdaq Stockholm, Meda is required to comply with certain Nasdaq Stockholm financial reporting requirements. The MTN program also provides for customary events of default (subject in certain cases to customary grace and cure periods), which include nonpayment, breach of covenants, payment defaults or acceleration of other indebtedness, failure to pay certain judgments and certain events of bankruptcy and insolvency. These covenants and events of default are subject to a number of important qualifications, limitations and exceptions that are described in the general terms and conditions of the MTN program. If an event of default with respect to the loans under the MTN program occurs, the principal amount of all of the loans under the MTN program then outstanding, plus accrued and unpaid interest, if any, to the date of acceleration, may become immediately due and payable.
The Loan Agreement contains customary affirmative covenants, including among others, covenants pertaining to the delivery of financial statements, notices of default and certain material events, maintenance of authorizations and compliance with laws, as well as customary negative covenants, including limitations on the incurrence of subsidiary indebtedness, disposals, liens, mergers and certain other corporate reconstructions and changes in Meda’s lines of business. Pursuant to the Loan Agreement, Meda must deliver to Svensk Exportkredit (i) within 60 days after the end of each consecutive three month period of its financial years, its unaudited consolidated financial statements for such three month period and (ii) within 120 days after the end of each of its financial years, its audited consolidated financial statements for such financial year. The Loan Agreement contains financial covenants limited to (i) a maximum senior net debt to EBITDA ratio, (ii) a maximum senior net debt to equity ratio and (iii) a minimum EBITDA interest coverage ratio.
Issuance of June 2016 Senior Notes
During the second quarter of 2016, in anticipation of the completion of the Offer, Mylan N.V. issued the June 2016 Senior Notes in a private offering exempt from the registration requirements of the Securities Act of 1933, as amended (the “Securities Act”), to qualified institutional buyers in accordance with Rule 144A and to persons outside of the U.S. pursuant to Regulation S under the Securities Act. The June 2016 Senior Notes were issued pursuant to an indenture, dated as of June 9, 2016 (the “Indenture”), among the Company, Mylan Inc., as guarantor (the “Guarantor”), and The Bank of New York Mellon, as trustee. The June 2016 Senior Notes were guaranteed by Mylan Inc. upon issuance. In addition, the Company entered into a registration rights agreement, dated as of June 9, 2016, pursuant to which the Company and Mylan Inc. will use commercially reasonable efforts to file a registration statement with respect to an offer to exchange each series of the June 2016 Senior Notes for new notes with the same aggregate principal amount and terms identical in all material respects and to cause the exchange offer registration statement to be declared effective by the SEC and to consummate the exchange offer not later than 365 days following the date of issuance of the June 2016 Senior Notes.
The Indenture contains covenants that, among other things, restrict the Company’s ability and the ability of certain of its subsidiaries to enter into sale and leaseback transactions; create liens; consolidate, merge or sell all or substantially all of the Company’s assets; and with respect to such subsidiaries only, guarantee certain of our or our other subsidiaries’ outstanding obligations or incur certain obligations without also guaranteeing our obligations under the June 2016 Senior Notes on a senior basis. The Indenture also provides for customary events of default (subject in certain cases to customary grace and cure periods), which include nonpayment, breach of covenants, payment defaults or acceleration of other indebtedness, failure to pay certain judgments and certain events of bankruptcy and insolvency. These covenants and events of default are subject to a number of important qualifications, limitations and exceptions that are described in the Indenture. If an event of default with respect to the June 2016 Senior Notes of a series occurs under the Indenture, the principal amount of all of the June 2016 Senior Notes of such series then outstanding, plus accrued and unpaid interest, if any, to the date of acceleration, may become immediately due and payable.
The 2.500% Senior Notes due 2019 mature on June 7, 2019, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 2.500% Senior Notes due 2019 bear interest at a rate of 2.500% per annum, accruing from June 9, 2016. Interest on the 2.500% Senior Notes due 2019 is payable semi-annually in arrears on June 7 and December 7 of each year, commencing on December 7, 2016. The 3.150% Senior Notes due 2021 mature on June 15, 2021, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 3.150% Senior Notes due 2021 bear interest at a rate of 3.150% per annum, accruing from June 9, 2016. Interest on the 3.150% Senior Notes due 2021 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016. The 3.950% Senior Notes due 2026 mature on June 15, 2026, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 3.950% Senior Notes due 2026 bear interest at a rate of 3.950% per annum, accruing from June 9, 2016. Interest on the 3.950% Senior Notes due 2026 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016. The 5.250% Senior Notes due 2046 mature on June 15, 2046, subject to earlier repurchase or redemption in accordance with the terms of the Indenture. The 5.250% Senior Notes due 2046 bear interest at a rate of 5.250% per annum, accruing from

June 9, 2016. Interest of the 5.250% Senior Notes due 2046 is payable semi-annually in arrears on June 15 and December 15 of each year, commencing on December 15, 2016.
At September 30, 2016, the outstanding balance of the 2.500% Senior Notes due 2019, 3.150% Senior Notes due 2021, 3.950% Senior Notes due 2026 and 5.250% Senior Notes due 2046 was $999.0 million, $2.25 billion, $2.23 billion and $999.8 million, respectively, which includes discounts of $1.0 million, $2.5 million, $16.9 million and $0.2 million, respectively. During the nine months ended September 30, 2016, the Company incurred approximately $47.9 million in financing fees, which were recorded as deferred financing costs in the Condensed Consolidated Balance Sheets.
2016 Bridge Credit Agreement
In connection with the Offer, on February 10, 2016, the Company entered into a Bridge Credit Agreement (the “2016 Bridge Credit Agreement”), among the Company, as borrower, Mylan Inc., as guarantor, Deutsche Bank AG Cayman Islands Branch, as administrative agent and a lender, Goldman Sachs Bank USA, as a lender, Goldman Sachs Lending Partners LLC, as a lender, and other lenders party thereto from time to time. The Company incurred total financing and ticking fees of approximately $45.2 million related to the 2016 Bridge Credit Agreement. During the first quarter of 2016, the Company wrote off approximately $3.0 million of financing fees related to the Tranche B Loans (as defined in the 2016 Bridge Credit Agreement) in conjunction with the termination of the Tranche B Loans. The remaining commitments under the 2016 Bridge Credit Agreement were permanently terminated in their entirety in connection with the completion of the offering of the June 2016 Senior Notes. As a result of the termination of the 2016 Bridge Credit Agreement, the Company expensed the remaining $30.2 million of unamortized financing fees related to the 2016 Bridge Credit Agreement to other expense, net in the Condensed Consolidated Statements of Operationsduring the second quarter of 2016.
Revolving Facility
On December 19, 2014, the Company entered into a revolving credit agreement, which was amended on May 1, 2015, and further amended on June 19, 2015 and October 28, 2015 (the “Revolving Credit Agreement”) with a syndicate of lenders, which contains a $1.65 billion revolving facility (the “Revolving Facility”), which expires on December 19, 2019. At September 30, 2016 and December 31, 2015, we had no amounts outstanding under the Revolving Facility. The interest rate under the Revolving Facility is LIBOR (determined in accordance withwhich also includes a $200 million subfacility for the Revolving Credit Agreement) plus 1.325% per annum. In addition, the Revolving Facility has a facility fee which is 0.175%. At September 30, 2016 and December 31, 2015, we had a totalissuance of $10.5 million and $11.1 million outstanding under existing letters of credit respectively. Additionally, asand a $175 million sublimit for swingline borrowings. As of September 30, 2016,March 31, 2017, we had $144.0$193.7 million available under the $150$200 million subfacility on our 2016 Revolving Facility for the issuance of letters of credit.
AmendmentIn addition to the 2016 Revolving Facility, 2015 Term Loans and 2014 Term Loan
On February 22, 2016,Mylan Pharmaceuticals Inc. (“MPI”), a wholly owned subsidiary of the Company, and Mylan Inc. (the “Borrower”) entered into (i) Amendment No. 3 (the “Revolving Amendment”) to the Revolving Credit Agreement dated December 19, 2014, as amended on May 1, 2015, further amended on June 19, 2015 and further amended on October 28, 2015 (as amended further by the Revolving Amendment, the “Revolving Credit Agreement”) which provided forhas a $1.65 billion revolving$400 million receivables facility (the “Revolving“Receivables Facility”), amongwhich will expire in January 2018. Although from time-to-time, the Borrower, the Company, certain lenders and issuing banks and Bank of America, N.A., as administrative agent, (ii) Amendment No. 2 (the “2015 Term Amendment”) to the Term Credit Agreement dated July 15, 2015, as amended on October 28, 2015 (as amended further by the 2015 Term Amendment, the “2015 Term Credit Agreement”) which provided for a delayed-draw term loan credit facility including loans totaling $1.6 billion (the “2015 Term Loans”), among the Borrower, the Company, certain lenders and PNC Bank, National Association, as administrative agent, and (iii) Amendment No. 3 (the “2014 Term Amendment”) to the Term Credit Agreement dated December 19, 2014, as amended on May 1, 2015 and further amended on October 28, 2015 (as amended further by the 2014 Term Amendment, the “2014 Term Credit Agreement”) which provided for an $800 million term loan (the “2014 Term Loan”), among the Borrower, the Company, certain lenders and Bank of America, N.A., as administrative agent. The Revolving Amendment, 2015 Term Amendment and 2014 Term Amendment provide that the Company’s acquisition of Meda constitutes a Qualified Acquisition (as defined in eachavailable amount of the Revolving Credit Agreement, the 2014 Term Credit AgreementReceivables Facility may be less than $400 million based on accounts receivable concentration limits and the 2015 Term Credit Agreement) and amends the event of default provisions to provide that any “change of control” put rights under any indebtedness of any Acquired Entity or Business (as defined in each of the Revolving Credit Agreement, the 2014 Term Credit Agreement and the 2015 Term Credit Agreement) or its subsidiaries that are triggered as a result of the acquisition of any Acquired Entity or Business will not result in an event of default so long as any such indebtedness that is put in accordance withother eligibility requirements. Under the terms of such indebtedness is paidthe Receivables Facility, MPI sells certain accounts receivable to Mylan Securitization LLC, a wholly owned special purpose entity which in turn sells a percentage of ownership interest in the receivables to financial institutions and commercial paper conduits sponsored by financial institutions. As of March 31, 2017, the Company had no amounts outstanding under the Receivables Facility.
At March 31, 2017, our long-term debt totaled $14.70 billion, as required bycompared to $15.20 billion at December 31, 2016. The decrease in long-term debt was due to the termsprepayment of such indebtedness.a portion of the 2016 Term Loans during the three months ended March 31, 2017. The total long-term debt balance at March 31, 2017 was comprised primarily of $1.05 billion of term loans, $148.6 million of Medium Term Notes acquired from Meda, $13.05 billion of fixed rate senior notes and $532.8 million of floating rate senior notes. In addition, at March 31, 2017, we had $227.2 million of long-term debt classified as current and payable within the next twelve months, as compared to $223.3 million at December 31, 2016. In addition to the current portion of long-term debt, the Company has significant debt maturities in the second and fourth quarters of 2018, as the 2.600% Senior Notes due 2018 mature in June 2018, the Floating Rate Euro Notes mature in November 2018 and the 3.000% Senior Notes due 2018 mature in December 2018. The Company intends to utilize available liquidity to fund these repayments.
For additional information regarding our debt agreements refer to Note 12Debt in Item 1 in this Form 10-Q.

Long-term Debt Maturity
Mandatory minimum repayments remaining on the outstanding notional amount of long-term debt at September 30, 2016, excluding the discounts and premiums,March 31, 2017 are as follows for each of the periods ending December 31:
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The Company’s next significant debt maturity is on November 29, 2016 as the Company’s 1.350% Senior Notes due 2016 mature. The Company intends to utilize available liquidity to fund the repayment of the 1.350% Senior Notes due 2016. In addition, the loans of $233.3 million under Meda’s Loan Agreement, due October 2017, are callable by the lender as a result of the completion of the Offer. The Company expects to use available liquidity to repay this amount if called.
The Company’s 2015 Term Loans 2014 Term Loan and 2016 Revolving Facility contain customary affirmative covenants for facilities of this type, including among others, covenants pertaining to the delivery of financial statements, notices of default and certain material events, maintenance of corporate existence and rights, property, and insurance and compliance with laws, as well as customary negative covenants for facilities of this type, including limitations on the incurrence of subsidiary indebtedness, liens, mergers and certain other fundamental changes, investments and loans, acquisitions, transactions with affiliates, payments of dividends and other restricted payments and changes in our lines of business. The 20152016 Term Loans 2014 Term Loan and 2016 Revolving Facility contain a maximum consolidated leverage ratio financial covenant. We have beenare compliant with these financial covenants during the nine months ended September 30, 2016,as of March 31, 2017, and we expect to remain in compliance for the next twelve months.
Collaboration and Licensing Agreements
We periodically enter into collaboration and licensing agreements with other pharmaceutical companies for the development, manufacture, marketing and/or sale of pharmaceutical products. Our significant collaboration agreements are focused on the development, manufacturing, supply and commercialization of multiple, high-value generic biologic compounds, insulin analog products and respiratory products. Under these agreements, we have future potential milestone payments and co-development expenses payable to third parties as part of our licensing, development and co-development programs. Payments under these agreements generally become due and are payable upon the satisfaction or achievement of certain developmental, regulatory or commercial milestones or as development expenses are incurred on defined projects. Milestone payment obligations are uncertain, including the prediction of timing and the occurrence of events triggering a future obligation and are not reflected as liabilities in the Condensed Consolidated Balance Sheets, except for milestone and royalty obligations reflected as acquisition contingent consideration. These agreements may also include potential sales based milestones and call for us to pay a percentage of amounts earned from the sale of the product as a royalty or a profit share. These sales based milestones or royalty obligations may be significant depending upon the level of commercial sales for each product.
Our most significant contingent payment relates to the potential future consideration related to our December 2011 acquisition of the respiratoryexclusive worldwide rights to develop, manufacture and commercialize a generic equivalent to GlaxoSmithKline’s Advair® Diskus and Seretide® Diskus incorporating Pfizer Inc.’s proprietary dry powder inhaler delivery platform.platform (the “respiratory delivery platform”). These payments are contingent upon the occurrence of certain future events and the ultimate success of the respective projects. Given the inherent uncertainty of these events, it is unclear when, if ever, we may be required to pay such amounts or pay amounts in excess of those accrued. The Company has also recorded contingent consideration related to the acquisition of the Topicals Business, the acquisition of Jaicertain female healthcare businesses from Famy Care Limited (such businesses, “Jai Pharma Limited,Limited”), the acquisition of Agila Specialties Private Limited (“Agila”) and certain other acquisitions. The amount of contingent consideration recorded was $651.5$566.0 million and $526.4$564.6 million at

September 30, 2016 March 31, 2017 and December 31, 2015,2016, respectively. Approximately $110 million related to the Strides Settlement is included in the balance at September 30, 2016. In addition, the Company expects to incur approximately $35 million to $40 million of annual accretion expense related to the increase in the net present value of the contingent consideration liability.
On January 8, 2016,In conjunction with the Company’s Generic Drug User Fee Agreement goal date, on March 28, 2017, the Company entered intoreceived a complete response letter from FDA regarding its Abbreviated New Drug Application for the respiratory delivery platform. As of March 31, 2017, the Company has an agreement with Momenta to develop, manufactureIPR&D asset of $347.2 million and commercialize up to sixrelated contingent consideration liability of Momenta’s current biosimilar candidates, including Momenta’s biosimilar candidate, ORENCIA® (abatacept). Mylan paid an up-front cash payment of $45 million to Momenta. Under the terms of the agreement, Momenta is eligible to receive additional contingent milestone payments of up to $200$436.1 million. The Company performed an analysis and Momenta will jointly be responsiblevaluation of the IPR&D asset and the fair value of the related contingent consideration liability through the use of a discounted cash flow model. The model contained certain key assumptions including: the expected product launch date, the number of competitors, the timing of competition and a discount

factor based on an industry specific weighted average cost of capital. Based on the analysis performed, the Company determined that the IPR&D asset was not impaired at March 31, 2017. Additionally, no significant fair value adjustment was required for product developmentthe contingent consideration. However, resolution of the matters with the FDA, market conditions and will equally shareother factors may result in significant changes in the costsprojections and profits relatedassumptions utilized in the discounted cash flow model, which could lead to material adjustments to the products. Under the agreement, Mylan will lead the worldwide commercialization efforts.
On November 2, 2016, the Company and Momenta announced that dosing had begun in a Phase 1 study to compare the pharmacokinetics, safety and immunogenicity of M834, a proposed bisoimilar or ORENCIA® (abatacept), to U.S. and European Union sourced ORENCIA® in normal healthy volunteers. Under the agreement, Momenta has achieved the milestone necessary to earn a $25 million payment from the Company which will be paid in the fourth quarter of 2016.recorded amounts.
We are actively pursuing, and are currently involved in, joint projects related to the development, distribution and marketing of both generic and branded products. Many of these arrangements provide for payments by us upon the attainment of specified milestones. While these arrangements help to reduce the financial risk for unsuccessful projects, fulfillment of specified milestones or the occurrence of other obligations may result in fluctuations in cash flows.
Other Commitments
We are involved in various legal proceedings that are considered normal to our business. While it is not possible to predict the outcome of such proceedings, an adverse outcome in any of these proceedings could materially affect our business, financial condition, results of operations, and cash flows and could cause the market value of our ordinary shares to decline. We have approximately $525$650 million accrued for legal contingencies, the majority of which relates to the Medicaid Drug Rebate Program Settlement.contingencies. For certain contingencies assumed in conjunction with the acquisition of the former Merck Generics business, Merck KGaA, the seller, has agreed to indemnify Mylan. Strides has also agreed to indemnify Mylan for certain contingencies related to our acquisition of Agila. The inability or denial of Merck KGaA, Strides Arcolab, or another indemnitor or insurer to pay on an indemnified claim could have a material adverse effect on our business, financial condition, results of operations, cash flows and/or ordinary share price.
We are continuously evaluating the potential acquisition of products, as well as companies, as a strategic part of our future growth. Consequently, we may utilize current cash reserves or incur additional indebtedness to finance any such acquisitions, which could impact future liquidity. In addition, on an ongoing basis, we review our operations including the evaluation of potential divestitures of products and businesses as part of our future strategy. Any divestitures could impact future liquidity.
Other Developments
Effective April 22, 2017, the Company entered into a six-year collective bargaining agreement with the United Steel, Paper and Forestry, Rubber, Manufacturing, Energy, Allied Industrial and Service Workers International Union and its Local Union 8-957 AFL-CIO which agreement governs certain production and maintenance employees at the Company’s largest manufacturing site in Morgantown, West Virginia. The agreement expires March 17, 2023.
ITEM 3.QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
For a discussion of the Company’s market risk, see “Item 7A. Quantitative and Qualitative Disclosures about Market Risk” in Mylan N.V.’s Annual Report filed on Form 10-K for the year ended December 31, 2015,2016, as amended.
ITEM 4.CONTROLS AND PROCEDURES
An evaluation was performed under the supervision and with the participation of the Company’s management, including the Principal Executive Officer and the Principal Financial Officer, of the effectiveness of the design and operation of the Company’s disclosure controls and procedures as of September 30, 2016.March 31, 2017. Based upon that evaluation, the Principal Executive Officer and the Principal Financial Officer concluded that the Company’s disclosure controls and procedures were effective.
Management identified the following change in the Company’s internal control over financial reporting (“ICFR”) that occurred during the quarter that has materially affected, or is reasonably likely to materially affect, the Company’s ICFR. During the quarter ended September 30, 2016,March 31, 2017, the Company begancontinued to implement and useutilize a new Enterprise Resource Planning (“ERP”) system in certain countries, which, when completed, will handle the business, financial and administrative processes for the Company. The Company has modified and will continue to modify its internal controls relating to its business and

financial processes throughout the entire ERP system implementation, which is expected to progress through the end of calendar 2017. While the Company believes that this new system and the related changes to internal controls will ultimately strengthen its ICFR, there are inherent risks in implementing any new ERP system and the Company will continue to evaluate and test control changes in order to provide certification as of its fiscal year ending December 31, 20162017 on the effectiveness of its ICFR.
During the three months ended September 30, 2016, the Company completed the acquisition
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PART II — OTHER INFORMATION
ITEM 1.LEGAL PROCEEDINGS
For information regarding legal proceedings, refer to Note 1819 ContingenciesLitigation, in the accompanying Notes to interim financial statements in this Quarterly Report.
ITEM 1A.
RISK FACTORS
Except as set forth below, thereThere have been no material changes in the Company’s risk factors from those disclosed in Mylan’s Annual Report on Form 10-K for the year ended December 31, 2015,2016, as amended, and Mylan’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2016.
Risks Related to the Business of Mylan
WE MAY BE ADVERSELY AFFECTED BY INCREASED SCRUTINY FROM THIRD PARTIES, INCLUDING GOVERNMENTS, OR NEGATIVE PUBLICITY WITH RESPECT TO MATTERS RELATING TO OUR PRODUCTS AND PRICING PRACTICES, AND OTHER MATTERS RELATED TO THE COMPANY, AND WE HAVE AND MAY CONTINUE TO EXPERIENCE PRICING PRESSURE ON THE PRICE OF CERTAIN OF OUR PRODUCTS DUE TO SOCIAL OR POLITICAL PRESSURE TO LOWER THE COST OF DRUGS, WHICH COULD REDUCE OUR REVENUE AND FUTURE PROFITABILITY.

There has been increased press coverage and increased scrutiny from third parties, including regulators, legislative bodies and enforcement agencies, with respect to matters relating to the Company’s business and pricing practices, and other matters related to the Company. This increased press coverage, public scrutiny and protests by some consumers have included assertions of wrongdoing by the Company which, regardless of the factual or legal basis for such assertions, have resulted in, and may continue to result in, investigations, and calls for investigations, by governmental agencies at both the federal and state level and have resulted in, and may continue to result in, claims brought against the Company by governmental agencies or by private parties or by regulators taking other measures that could have a negative effect on the Company’s business. It is not possible at this time to predict the ultimate outcome of any such investigations or claims or what other investigations or lawsuits or regulatory responses may result from such assertions, or their impact on the Company’s business, financial condition, results of operations, cash flows, and/or ordinary share price. Any such investigation or claim could also result in reputational harm and reduced market acceptance and demand for our products, could harm our ability to market our products in the future, could cause us to incur significant expense, could cause our senior management to be distracted from execution of our business strategy, and could have a material adverse effect on our business, financial condition, results of operations and growth prospects.
There has also recently been intense publicity regarding the pricing of pharmaceuticals more generally, including publicity and pressure resulting from prices charged by competitors and peer companies for new products as well as price increases by competitors and peer companies on older products that the public has deemed excessive. We have experienced and may continue to experience downward pricing pressure on the price of certain of our products due to social or political pressure to lower the cost of drugs, which could reduce our revenue and future profitability.
Accompanying the press and media coverage of pharmaceutical pricing practices and public complaints about the same, there has been increasing U.S. federal and state legislative and enforcement interest with respect to drug pricing. In particular, U.S. federal prosecutors recently issued subpoenas to pharmaceutical companies, including Mylan, seeking information about their drug pricing practices, among other issues, and members of the U.S. Congress have sought information from certain pharmaceutical companies, including Mylan, relating to drug-price increases. Additionally, there have been several recent U.S. Congressional inquiries and proposed bills designed to, among other things, bring more transparency to drug pricing, review the relationship between pricing and manufacturer patient programs, and reform government program reimbursement methodologies for drugs. For example, in late 2015 the U.S. House of Representatives formed an Affordable Drug Pricing Task Force to advance legislation intended to control pharmaceutical drug costs and investigate pharmaceutical drug pricing. Since then, both the U.S. House of Representatives and the U.S. Senate have conducted numerous hearings with respect to pharmaceutical drug pricing practices, including in connection with the investigation of specific price increases by several pharmaceutical companies such as Mylan. In addition to the effects of any investigations or claims brought against the Company described above, our revenue and future profitability could also be negatively affected if any such inquiries, of us or

of other pharmaceutical companies or the industry more generally, were to result in legislative or regulatory proposals that limit our ability to increase the prices of our products.
Any of the events or developments described above could have a material adverse impact on our business, financial condition or results of operations, as well as on our reputation.amended.
ITEM 6. EXHIBITS
10.1Facilities Agreement, dated December 17, 2014, among Meda AB (publ),Amendment to Amended and Restated 2003 Long-Term Incentive Plan, adopted as borrower, certain lenders party thereto, and Danske Bank A/S, as agent.of February 23, 2017*
  
10.2Amendment Letter, dated October 29, 2015, to
Form of Restricted Stock Unit Award Agreement under the Facilities Agreement, dated December 17, 2014, among Meda AB (publ), as borrower, certain lenders party thereto,2003 Long-Term Incentive Plan for Heather Bresch and Danske Bank A/S, as agent.Rajiv Malik for awards granted on or after February 23, 2017*
  
10.3Amendment
Form of Performance-Based Restricted Stock Unit Award Agreement under the 2003 Long-Term Incentive Plan for Heather Bresch and Waiver Letter, dated August 30, 2016, to the Facilities Agreement, dated December 17, 2014, as amended by the Amendment Letter, dated October 29, 2015, among Meda AB (publ), as borrower, certain lenders party thereto, and Danske Bank A/S, as agent.Rajiv Malik for awards granted on or after February 23, 2017*
  
10.4
LoanForm of Waiver Letter with respect to Specified Award Agreements by and between Mylan N.V and Heather Bresch and Rajiv Malik, February 23, 2017*
10.5Executive Employment Agreement, dated September 17, 2014,March 24, 2017 and effective April 1, 2017, between Meda AB (publ), as borrower,Mylan Inc. and AB Svensk Exportkredit (publ), as lender.

Daniel M. Gallagher*
10.6Transition and Succession Agreement, dated March 24, 2017, between Mylan Inc. and Daniel M. Gallagher*
10.7Form of Performance-Based Restricted Stock Unit Award Agreement under the One-Time Special Five-Year Performance-Based Realizable Value Incentive Program for Daniel M. Gallagher*
  
31.1Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
  
31.2Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
  
32Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
  
101.INSXBRL Instance Document
  
101.SCHXBRL Taxonomy Extension Schema
  
101.CALXBRL Taxonomy Extension Calculation Linkbase
  
101.DEFXBRL Taxonomy Definition Linkbase
  
101.LABXBRL Taxonomy Extension Label Linkbase
  
101.PREXBRL Taxonomy Extension Presentation Linkbase
  
*Denotes management contract or compensatory plan or arrangement.



SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
  
Mylan N.V.
(Registrant)
   
 By:/s/ Heather BreschHEATHER BRESCH
  Heather Bresch
  Chief Executive Officer
  (Principal Executive Officer)
November 9, 2016May 10, 2017
 
  /s/ KennethKENNETH S. ParksPARKS
  Kenneth S. Parks
  Chief Financial Officer
  (Principal Financial Officer)
November 9, 2016May 10, 2017


EXHIBIT INDEX
10.1Facilities Agreement, dated December 17, 2014, among Meda AB (publ),Amendment to Amended and Restated 2003 Long-Term Incentive Plan, adopted as borrower, certain lenders party thereto, and Danske Bank A/S, as agent.of February 23, 2017*
  
10.2Amendment Letter, dated October 29, 2015, to
Form of Restricted Stock Unit Award Agreement under the Facilities Agreement, dated December 17, 2014, among Meda AB (publ), as borrower, certain lenders party thereto,2003 Long-Term Incentive Plan for Heather Bresch and Danske Bank A/S, as agent.Rajiv Malik for awards granted on or after February 23, 2017*
  
10.3Amendment
Form of Performance-Based Restricted Stock Unit Award Agreement under the 2003 Long-Term Incentive Plan for Heather Bresch and Waiver Letter, dated August 30, 2016, to the Facilities Agreement, dated December 17, 2014, as amended by the Amendment Letter, dated October 29, 2015, among Meda AB (publ), as borrower, certain lenders party thereto, and Danske Bank A/S, as agent.Rajiv Malik for awards granted on or after February 23, 2017*
  
10.4LoanForm of Waiver Letter with respect to Specified Award Agreements by and between Mylan N.V and Heather Bresch and Rajiv Malik, February 23, 2017*
10.5Executive Employment Agreement, dated September 17, 2014,March 24, 2017 and effective April 1, 2017, between Meda AB (publ), as borrower,Mylan Inc. and AB Svensk Exportkredit (publ), as lender.
Daniel M. Gallagher*
10.6Transition and Succession Agreement, dated March 24, 2017, between Mylan Inc. and Daniel M. Gallagher*
10.7Form of Performance-Based Restricted Stock Unit Award Agreement under the One-Time Special Five-Year Performance-Based Realizable Value Incentive Program for Daniel M. Gallagher*
  
31.1Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
  
31.2Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
  
32Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
  
101.INSXBRL Instance Document
  
101.SCHXBRL Taxonomy Extension Schema
  
101.CALXBRL Taxonomy Extension Calculation Linkbase
  
101.DEFXBRL Taxonomy Definition Linkbase
  
101.LABXBRL Taxonomy Extension Label Linkbase
  
101.PREXBRL Taxonomy Extension Presentation Linkbase
  
*Denotes management contract or compensatory plan or arrangement.


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