UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 10-Q
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended June 30, 20212022
OR
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from_____________to___________from _____________to___________                 
Commission file number 001-39695
VIATRIS INC.
(Exact name of registrant as specified in its charter)
Delaware83-4364296
(State or other jurisdiction
of incorporation or organization)
(I.R.S. Employer
Identification No.)
1000 Mylan Boulevard, Canonsburg, Pennsylvania 15317
(Address of principal executive offices)
(724) 514-1800
(Registrant’s telephone number, including area code)
Securities registered pursuant to Section 12(b) of the Act:
Title of Each Class:Trading Symbol(s)Name of Each Exchange on Which Registered:
Common Stock, par value $0.01 per shareVTRSThe NASDAQ Stock Market

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      No  
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted 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 such files).    Yes      No  
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filerAccelerated filer
Non-accelerated filerSmaller reporting company
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use 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  
Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date.
The number of shares of common stock outstanding, par value $0.01 per share, of the registrant as of August 4, 20213, 2022 was 1,209,290,460.1,212,580,940.


Table of Contents
VIATRIS INC. AND SUBSIDIARIES
INDEX TO FORM 10-Q
For the Quarterly Period Ended
June 30, 20212022
  
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.

















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Glossary of Defined Terms

Unless the context requires otherwise, references to “Viatris,” “the Company,” “we,” “us” or “our” in this Form 10-Q (defined below) refer to Viatris Inc. and its subsidiaries. We also have used several other terms in this Form 10-Q, most of which are explained or defined below. Some amounts in this Form 10-Q may not add due to rounding.


2003 LTIPMylan N.V. Amended and Restated 2003 Long-Term Incentive Plan
20202021 Form 10-KViatris’ annual report on Form 10-K for the fiscal year ended December 31, 2020,2021, as amended
2020 Revolving FacilityThe revolving credit facility available pursuant to the revolving credit agreement, dated as of June 16, 2020, by and among Viatris, certain lenders and issuing banks from time to time party thereto and Bank of America, N.A., as administrative agent and repaid in full in July 2021
2021 Revolving FacilityThe $4.0 billion revolving facility dated as of July 1, 2021, by and among Viatris, certain lenders and issuing banks from time to time party thereto and Bank of America, N.A., as administrative agent
Adjusted EBITDANon-GAAP financial measure that the Company believes is appropriate to provide information to investors - EBITDA (defined below) is further adjusted for share-based compensation expense, litigation settlements, and other contingencies, net, restructuring and other special items
ANDAAbbreviated New Drug Application
AOCEAccumulated other comprehensive earnings
APIsActive pharmaceutical ingredients
ARVAntiretroviral medicines
ASCAccounting Standards Codification
AspenAspen Global Incorporated
ASUAccounting Standards Update
BioconBiocon Limited
Biocon BiologicsBiocon Biologics Limited, a majority owned subsidiary of Biocon
Biocon Biologics TransactionThe pending transaction between Viatris and Biocon Biologics pursuant to which Viatris will contribute its biosimilars portfolio to Biocon Biologics
Biocon AgreementThe transaction agreement between Viatris and Biocon Biologics, dated February 27, 2022, relating to the Biocon Biologics Transaction
BiogenBiogen MA Inc. and Biogen International GmbH, collectively
Business Combination AgreementBusiness Combination Agreement, dated as of July 29, 2019, as amended from time to time, among Viatris, Mylan, Pfizer and certain of their affiliates
CATCompetition Appeals Tribunal
CJEUEuropean Court of Justice
clean energy investmentsUsed to define the three equity method investments the Company has in limited liability companies that own refined coal production plants whose activities qualify for income tax credits under Section 45 of the Code
CMACompetition and Markets Authority
CodeThe U.S. Internal Revenue Code of 1986, as amended
CombinationRefers to Mylan combining with Pfizer's Upjohn Business in a Reverse Morris Trust transaction to form Viatris on November 16, 2020
Commercial Paper ProgramThe $1.65 billion unsecured commercial paper program entered into as of November 16, 2020 by Viatris, as issuer, Mylan Inc., Utah Acquisition Sub Inc. and Mylan II B.V., as guarantors, and certain dealers from time to time
CommissionEuropean Commission
COVID-19Novel coronavirus disease of 2019
CP NotesUnsecured, short-term commercial paper notes issued pursuant to the Commercial Paper Program
DCGIDrug Controller General of India
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Developed Markets segmentViatris’ business segment that includes our operations primarily in the following markets: North America and Europe
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DistributionPfizer's distribution to Pfizer stockholders all the issued and outstanding shares of Upjohn Inc.
DOJU.S. Department of Justice
DRIPDividend Reinvestment and Share Purchase Plan
EBITDANon-GAAP financial measure that the Company believes is appropriate to provide information to investors - U.S. GAAP net earnings (loss) adjusted for net contribution attributable to equity method investments, income tax provision (benefit), interest expense and depreciation and amortization
EDPAU.S. District Court for the Eastern District of Pennsylvania
Emerging Markets segmentViatris’ business segment that includes, but is not limited to, our operations primarily in the following markets: Parts of Asia, the Middle East, South and Central America, Africa, and Eastern Europe
ERP systemEnterprise resource planning system
EUEuropean Union
Exchange ActSecurities Exchange Act of 1934, as amended
FASBFinancial Accounting Standards Board
FCAFinancial Conduct Authority in the U.K.
FDAU.S. Food and Drug Administration
Form 10-QThis quarterly report on Form 10-Q for the quarterly period ended June 30, 20212022
Greater China segmentViatris’ business segment that includes our operations primarily in the following markets: China, Taiwan and Hong Kong
GxGeneric drugs
IPRInter Partes review
IRSU.S. Internal Revenue Service
IRS RulingThe private letter ruling issued by the IRS to Pfizer with respect to the Combination, dated as of March 17, 2020
ITInformation technology
JANZ segmentViatris’ business segment that includes our operations primarily in the following markets: Japan, Australia and New Zealand
LIBORLondon Interbank Offered Rate
LillyEli Lilly and Company
maximum leverage ratioThe maximum consolidated leverage ratio financial covenant requiring maintenance of a maximum ratio of consolidated total indebtedness as of the end of any quarter to consolidated EBITDA for the trailing four quarters as defined in the related credit agreements from time to time
MDLMultidistrict litigation
MPIMylan PharmaceuticalPharmaceuticals Inc.
MylanMylan N.V. and its subsidiaries
Mylan IIMylan II B.V.;, a company incorporated under the laws of the Netherlands and an indirect wholly owned subsidiary of Viatris, in which legacy Mylan merged with and into
Mylan Inc. SeniorEuro NotesThe 2.125% Senior Notes due 2025 issued by Mylan Inc., which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan II B.V., Viatris Inc. and Utah Acquisition Sub Inc.
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Mylan Inc. U.S. Dollar NotesThe 4.200% Senior Notes due 2023, 3.125% Senior Notes due 2023, 4.550% Senior Notes due 2028, 5.400% Senior Notes due 2043 and 5.200% Senior Notes due 2048 issued by Mylan Inc., which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan II B.V., Viatris Inc. and Utah Acquisition Sub Inc.
Mylan SecuritizationMylan Securitization LLC
NASDAQThe NASDAQ Stock Market
NDANew drug application
NHSNational Health Services
Note Securitization FacilityThe note securitization facility entered into in July 2021 for borrowings up to $200 million and expiring in August 2022
OTCOver-the-counter
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PfizerPfizer Inc.
PlanViatris Inc. 2020 Stock Incentive Plan
PMSPharmascience Inc.
PSUsPerformance awards
PTABU.S. Patent Trial and Appeal Board
R&DResearch and development
Receivables FacilityThe $400 million accounts receivable entered into in August 2020 and expiring in April 20222025
Registered Upjohn NotesThe 1.650% Senior Notes due 2025, 2.300% Senior Notes due 2027, 2.700% Senior Notes due 2030, 3.850% Senior Notes due 2040 and 4.000% Senior Notes due 2050 originally issued on October 29, 2021 registered with the SEC in exchange for the corresponding Unregistered Upjohn U.S. Dollar Notes in a similar aggregate principal amount and with terms substantially identical to the corresponding Unregistered Upjohn U.S. Dollar Notes and fully and unconditionally guaranteed by Mylan Inc., Mylan II and Utah Acquisition Sub Inc.
respiratory delivery platformPfizer’s proprietary dry powder inhaler delivery platform
restricted stock awardsThe Company’s nonvested restricted stock and restricted stock unit awards, including PSUs
Revolving FacilityThe $4.0 billion revolving facility dated as of July 1, 2021, by and among Viatris, certain lenders and issuing banks from time to time party thereto and Bank of America, N.A., as administrative agent
RICORacketeer Influenced and Corrupt Organizations Act
RSUsThe Company's unvested restricted stock unit awards
SanofiSanofi-Aventis U.S., LLC
SARsStock Appreciation Rights
SDNYU.S. District Court for the Southern District of New York
SECU.S. Securities and Exchange Commission
Securities ActSecurities Act of 1933, as amended
Senior U.S. Dollar NotesThe Upjohn U.S. Dollar Notes, the Utah SeniorU.S. Dollar Notes and the Mylan Inc. SeniorU.S. Dollar Notes, collectively
SeparationPfizer's transfer to Upjohn of substantially all the assets and liabilities comprising the Upjohn Business
Separation and Distribution AgreementSeparation and Distribution Agreement between Viatris and Pfizer, dated as of July 29, 2019, as amended from time to time
SG&ASelling, general and administrative expenses
SOFRSecured overnight financial rate
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Stock awardsStock options and SARs
TevaTeva Pharmaceutical Industries Ltd.
TSATransition service agreements
U.K.United Kingdom
U.S.United States
U.S. GAAPAccounting principles generally accepted in the U.S.
Unregistered Upjohn U.S. Dollar NotesThe 1.650% Senior Notes due 2025, 2.300% Senior Notes due 2027, 2.700% Senior Notes due 2030, 3.850% Senior Notes due 2040 and 4.000% Senior Notes due 2050 originally issued on June 22, 2020 by Upjohn Inc. (now Viatris Inc.) in a private offering exempt from the registration requirements of the Securities Act and fully and unconditionally guaranteed by Mylan Inc., Mylan II and Utah Acquisition Sub Inc.
UpjohnUpjohn Inc., a wholly owned subsidiary of Pfizer prior to the Distribution, that combined with Mylan and was renamed Viatris Inc.
Upjohn BusinessPfizer’s off-patent branded and generic established medicines business that, in connection with the Combination, was separated from Pfizer and combined with Mylan to form Viatris
USD Term Loan AgreementUpjohn U.S. Dollar NotesSenior unsecured notes denominated in U.S. dollars and originally issued by Upjohn Inc. or Viatris Inc. pursuant to an indenture dated June 22, 2020 and fully and unconditionally guaranteed by Mylan Inc., Mylan II B.V. and Utah Acquisition Sub Inc.
Utah Acquisition SubThe $600 million delayed draw term loan credit agreement, dated asUtah Acquisition Sub Inc., a Delaware corporation and an indirect wholly owned subsidiary of June 16, 2020 by and among Viatris Mizuho Bank, Ltd. and MUFG Bank, Ltd., as administrative agent, and repaid in full in July 2021
Utah Euro NotesThe 2.250% Senior Notes due 2024 and 3.125% Senior Notes due 2028 issued by Utah Acquisition Sub Inc., which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan Inc., Viatris Inc. and Mylan II B.V.
Utah U.S. Dollar NotesThe 3.150% Senior Notes due 2021, 3.950% Senior Notes due 2026 and 5.250% Senior Notes due 2046 issued by Utah Acquisition Sub Inc., which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan Inc., Viatris Inc. and Mylan II B.V.
ViatrisViatris Inc., formerly known as Upjohn Inc. prior to the completion of the Combination
YEN Term Loan AgreementFacilityThe ¥40 billion term loan agreement dated as of July 1, 2021, by and among Viatris, MizuhoMUFG Bank, Ltd. and MUFGMizuho Bank, Ltd., as administrative agent
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PART I — FINANCIAL INFORMATION

VIATRIS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Operations
(Unaudited; in millions, except per share amounts)
Three Months EndedSix Months Ended Three Months EndedSix Months Ended
June 30,June 30,June 30,June 30,
2021202020212020 2022202120222021
Revenues:Revenues:Revenues:
Net salesNet sales$4,561.7 $2,695.9 $8,961.8 $5,284.1 Net sales$4,105.4 $4,561.7 $8,283.6 $8,961.8 
Other revenuesOther revenues16.1 35.3 46.3 66.3 Other revenues11.4 16.1 24.9 46.3 
Total revenuesTotal revenues4,577.8 2,731.2 9,008.1 5,350.4 Total revenues4,116.8 4,577.8 8,308.5 9,008.1 
Cost of salesCost of sales3,250.1 1,705.5 6,553.1 3,418.6 Cost of sales2,413.5 3,250.1 4,834.0 6,553.1 
Gross profitGross profit1,327.7 1,025.7 2,455.0 1,931.8 Gross profit1,703.3 1,327.7 3,474.5 2,455.0 
Operating expenses:Operating expenses:Operating expenses:
Research and developmentResearch and development147.7 156.3 331.8 270.5 Research and development162.6 147.7 304.9 331.8 
Selling, general and administrativeSelling, general and administrative1,204.8 719.4 2,391.3 1,324.8 Selling, general and administrative981.1 1,204.8 1,896.4 2,391.3 
Litigation settlements and other contingencies, netLitigation settlements and other contingencies, net23.0 15.8 45.9 17.6 Litigation settlements and other contingencies, net10.9 23.0 17.1 45.9 
Total operating expensesTotal operating expenses1,375.5 891.5 2,769.0 1,612.9 Total operating expenses1,154.6 1,375.5 2,218.4 2,769.0 
(Loss) earnings from operations(47.8)134.2 (314.0)318.9 
Earnings (loss) from operationsEarnings (loss) from operations548.7 (47.8)1,256.1 (314.0)
Interest expenseInterest expense167.1 116.2 336.1 236.1 Interest expense145.9 167.1 292.1 336.1 
Other expense (income), net4.2 (2.0)10.3 32.1 
(Loss) earnings before income taxes(219.1)20.0 (660.4)50.7 
Income tax provision (benefit)60.1 (19.4)656.4 (9.5)
Net (loss) earnings$(279.2)$39.4 $(1,316.8)$60.2 
(Loss) earnings per share attributable to Viatris Inc. shareholders
Other expense, netOther expense, net13.5 4.2 47.2 10.3 
Earnings (loss) before income taxesEarnings (loss) before income taxes389.3 (219.1)916.8 (660.4)
Income tax provisionIncome tax provision75.4 60.1 203.7 656.4 
Net earnings (loss)Net earnings (loss)$313.9 $(279.2)$713.1 $(1,316.8)
Earnings (loss) per share attributable to Viatris Inc. shareholdersEarnings (loss) per share attributable to Viatris Inc. shareholders
BasicBasic$(0.23)$0.08 $(1.09)$0.12 Basic$0.26 $(0.23)$0.59 $(1.09)
DilutedDiluted$(0.23)$0.08 $(1.09)$0.12 Diluted$0.26 $(0.23)$0.59 $(1.09)
Weighted average shares outstanding:Weighted average shares outstanding:Weighted average shares outstanding:
BasicBasic1,208.8 516.9 1,208.2 516.7 Basic1,212.3 1,208.8 1,211.4 1,208.2 
DilutedDiluted1,208.8 517.2 1,208.2 517.1 Diluted1,217.1 1,208.8 1,215.1 1,208.2 


See Notes to Condensed Consolidated Financial Statements
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VIATRIS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Comprehensive Loss
(Unaudited; in millions)
 Three Months EndedSix Months Ended
June 30,June 30,
 2021202020212020
Net (loss) earnings$(279.2)$39.4 $(1,316.8)$60.2 
Other comprehensive earnings (loss), before tax:
Foreign currency translation adjustment160.7 452.0 (560.5)(204.6)
Change in unrecognized gain and prior service cost related to defined benefit plans72.5 6.6 73.3 5.0 
Net unrecognized gain (loss) on derivatives in cash flow hedging relationships12.4 18.7 15.7 (32.7)
Net unrecognized (loss) gain on derivatives in net investment hedging relationships(77.4)(47.3)150.0 (5.0)
Net unrealized gain (loss) on marketable securities0.2 0.6 (0.7)0.8 
Other comprehensive earnings (loss), before tax168.4 430.6 (322.2)(236.5)
Income tax (benefit) provision(12.2)2.0 24.8 (8.8)
Other comprehensive earnings (loss), net of tax180.6 428.6 (347.0)(227.7)
Comprehensive (loss) earnings$(98.6)$468.0 $(1,663.8)$(167.5)
 Three Months EndedSix Months Ended
June 30,June 30,
 2022202120222021
Net earnings (loss)$313.9 $(279.2)$713.1 $(1,316.8)
Other comprehensive (loss) earnings, before tax:
Foreign currency translation adjustment(1,149.9)160.7 (1,619.1)(560.5)
Change in unrecognized gain (loss) and prior service cost related to defined benefit plans0.5 72.5 (2.1)73.3 
Net unrecognized gain on derivatives in cash flow hedging relationships17.6 12.4 17.8 15.7 
Net unrecognized gain (loss) on derivatives in net investment hedging relationships384.4 (77.4)585.7 150.0 
Net unrealized (loss) gain on marketable securities(1.0)0.2 (2.7)(0.7)
Other comprehensive (loss) earnings, before tax(748.4)168.4 (1,020.4)(322.2)
Income tax provision (benefit)89.8 (12.2)134.5 24.8 
Other comprehensive (loss) earnings, net of tax(838.2)180.6 (1,154.9)(347.0)
Comprehensive loss$(524.3)$(98.6)$(441.8)$(1,663.8)



See Notes to Condensed Consolidated Financial Statements
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VIATRIS INC. AND SUBSIDIARIES
Condensed Consolidated Balance Sheets
(Unaudited in millions, except share and per share amounts)
June 30,
2021
December 31,
2020
June 30,
2022
December 31,
2021
ASSETSASSETSASSETS
AssetsAssetsAssets
Current assets:Current assets:Current assets:
Cash and cash equivalentsCash and cash equivalents$673.9 $844.4 Cash and cash equivalents$664.7 $701.2 
Accounts receivable, netAccounts receivable, net4,478.7 4,843.8 Accounts receivable, net3,736.2 4,266.4 
InventoriesInventories4,487.6 5,471.9 Inventories3,612.5 3,977.7 
Prepaid expenses and other current assetsPrepaid expenses and other current assets2,109.6 1,707.4 Prepaid expenses and other current assets1,697.7 1,957.6 
Assets held for saleAssets held for sale1,465.4 — 
Total current assetsTotal current assets11,749.8 12,867.5 Total current assets11,176.5 10,902.9 
Property, plant and equipment, netProperty, plant and equipment, net3,171.4 3,459.9 Property, plant and equipment, net3,083.9 3,188.6 
Intangible assets, netIntangible assets, net27,863.7 29,683.2 Intangible assets, net24,101.1 26,134.2 
GoodwillGoodwill11,990.4 12,347.0 Goodwill10,523.0 12,113.7 
Deferred income tax benefit - noncurrent2,183.7 2,147.9 
Deferred income tax benefitDeferred income tax benefit1,243.2 1,332.7 
Other assetsOther assets1,025.1 1,047.5 Other assets997.4 1,170.7 
Total assetsTotal assets$57,984.1 $61,553.0 Total assets$51,125.1 $54,842.8 
LIABILITIES AND EQUITYLIABILITIES AND EQUITYLIABILITIES AND EQUITY
LiabilitiesLiabilitiesLiabilities
Current liabilities:Current liabilities:Current liabilities:
Accounts payableAccounts payable$1,800.2 $1,904.2 Accounts payable$1,670.1 $1,657.4 
Short-term borrowingsShort-term borrowings1,300.5 1,100.9 Short-term borrowings1,019.7 1,493.0 
Income taxes payableIncome taxes payable636.0 288.6 Income taxes payable125.7 236.9 
Current portion of long-term debt and other long-term obligationsCurrent portion of long-term debt and other long-term obligations2,184.4 2,308.5 Current portion of long-term debt and other long-term obligations768.2 1,877.5 
Liabilities held for saleLiabilities held for sale285.1 — 
Other current liabilitiesOther current liabilities4,211.5 4,960.7 Other current liabilities3,812.4 4,619.6 
Total current liabilitiesTotal current liabilities10,132.6 10,562.9 Total current liabilities7,681.2 9,884.4 
Long-term debtLong-term debt20,917.0 22,429.2 Long-term debt19,206.4 19,717.1 
Deferred income tax liabilityDeferred income tax liability3,485.7 3,123.7 Deferred income tax liability2,617.9 2,815.0 
Other long-term obligationsOther long-term obligations2,241.9 2,483.1 Other long-term obligations1,814.2 1,933.6 
Total liabilitiesTotal liabilities36,777.2 38,598.9 Total liabilities31,319.7 34,350.1 
EquityEquityEquity
Viatris Inc. shareholders’ equityViatris Inc. shareholders’ equityViatris Inc. shareholders’ equity
Common stock — par value $0.01 per share as of June 30, 2021 and December 31, 2020:
Shares authorized: 3,000,000,000 as of June 30, 2021 and December 31, 2020
Shares issued: 1,209,212,338 and 1,206,895,644 as of June 30, 2021 and December 31, 202012.1 12.1 
Common stock: $0.01 par value, 3,000,000,000 shares authorized; shares issued and outstanding: 1,212,447,457 and 1,209,507,463, respectivelyCommon stock: $0.01 par value, 3,000,000,000 shares authorized; shares issued and outstanding: 1,212,447,457 and 1,209,507,463, respectively12.1 12.1 
Additional paid-in capitalAdditional paid-in capital18,489.9 18,438.8 Additional paid-in capital18,585.7 18,536.1 
Retained earningsRetained earnings3,909.9 5,361.2 Retained earnings4,106.8 3,688.8 
Accumulated other comprehensive lossAccumulated other comprehensive loss(1,205.0)(858.0)Accumulated other comprehensive loss(2,899.2)(1,744.3)
Total equityTotal equity21,206.9 22,954.1 Total equity19,805.4 20,492.7 
Total liabilities and equityTotal liabilities and equity$57,984.1 $61,553.0 Total liabilities and equity$51,125.1 $54,842.8 

See Notes to Condensed Consolidated Financial Statements
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VIATRIS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Equity
(Unaudited; in millions, except share amounts)
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
 Common StockTreasury Stock
 SharesCostSharesCost
Balance at March 31, 20211,208,530,970 $12.1 $18,464.6 $4,323.6 $$(1,385.6)$21,414.7 
Net loss— — — (279.2)— — — (279.2)
Other comprehensive earnings, net of tax— — — — — — 180.6 180.6 
Issuance of restricted stock and stock options exercised, net681,368 — — — — — — 
Taxes related to the net share settlement of equity awards— — (5.7)— — — — (5.7)
Share-based compensation expense— — 31.0 — — — — 31.0 
Cash dividends declared, $0.11 per common share— — — (134.5)— — — (134.5)
Balance at June 30, 20211,209,212,338 $12.1 $18,489.9 $3,909.9 $$(1,205.0)$21,206.9 
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
Common StockTreasury Stock
SharesCostSharesCost
Balance at December 31, 20201,206,895,644 $12.1 $18,438.8 $5,361.2 $$(858.0)$22,954.1 
Net loss— — — (1,316.8)— — — (1,316.8)
Other comprehensive loss, net of tax— — — — — — (347.0)(347.0)
Issuance of restricted stock and stock options exercised, net2,316,694 — — — — 
Taxes related to the net share settlement of equity awards— — (12.6)— — — — (12.6)
Share-based compensation expense— — 63.7 — — — — 63.7 
Cash dividends declared, $0.11 per common share— — — (134.5)— — — (134.5)
Balance at June 30, 20211,209,212,338 $12.1 $18,489.9 $3,909.9 $$(1,205.0)$21,206.9 
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
 Common StockTreasury Stock
 SharesCostSharesCost
Balance at March 31, 20221,212,323,483 $12.1 $18,555.1 $3,941.5 — $— $(2,061.0)$20,447.7 
Net earnings— — — 313.9 — — — 313.9 
Other comprehensive loss, net of tax— — — — — — (838.2)(838.2)
Issuance of restricted stock and stock options exercised, net64,292 — — — — — — — 
Taxes related to the net share settlement of equity awards— — 0.5 — — — — 0.5 
Share-based compensation expense— — 29.4 — — — — 29.4 
Issuance of common stock59,682 — 0.7 — — — — 0.7 
Cash dividends declared, $0.12 per common share— — — (148.6)— — — (148.6)
Balance at June 30, 20221,212,447,457 $12.1 $18,585.7 $4,106.8 — $— $(2,899.2)$19,805.4 
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
Common StockTreasury Stock
SharesCostSharesCost
Balance at December 31, 20211,209,507,463 $12.1 $18,536.1 $3,688.8 — $— $(1,744.3)$20,492.7 
Net earnings— — — 713.1 — — — 713.1 
Other comprehensive loss, net of tax— — — — — — (1,154.9)(1,154.9)
Issuance of restricted stock and stock options exercised, net2,880,312 — — — — — — — 
Taxes related to the net share settlement of equity awards— — (8.8)— — — — (8.8)
Share-based compensation expense— — 57.7 — — — — 57.7 
Issuance of common stock59,682 — 0.7 — — — — 0.7 
Cash dividends declared, $0.24 per common share— — — (295.1)— — — (295.1)
Balance at June 30, 20221,212,447,457 $12.1 $18,585.7 $4,106.8 — $— $(2,899.2)$19,805.4 
See Notes to Condensed Consolidated Financial Statements
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Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
 
Ordinary Shares (1)
Treasury Stock
 SharesCostSharesCost
Balance at March 31, 2020541,542,294 $6.1 $8,657.9 $6,051.9 24,598,074 $(999.7)$(2,453.5)$11,262.7 
Net earnings— — — 39.4 — — — 39.4 
Other comprehensive earnings, net of tax— — — — — — 428.6 428.6 
Issuance of restricted stock and stock options exercised, net3,014 — — — — — — 
Share-based compensation expense— — 15.3 — — — — 15.3 
Other— — — 0.2 — — — 0.2 
Balance at June 30, 2020541,545,308 $6.1 $8,673.2 $6,091.5 24,598,074 $(999.7)$(2,024.9)$11,746.2 
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
Ordinary Shares (1)
Treasury Stock
SharesCostSharesCost
Balance at December 31, 2019540,746,871 $6.1 $8,643.5 $6,031.1 24,598,074 $(999.7)$(1,797.2)$11,883.8 
Net earnings— — — 60.2 — — — 60.2 
Other comprehensive loss, net of tax— — — — — — (227.7)(227.7)
Issuance of restricted stock and stock options exercised, net798,437 — 0.6 — — — — 0.6 
Taxes related to the net share settlement of equity awards— — (5.6)— — — — (5.6)
Share-based compensation expense— — 34.7 — — — — 34.7 
Other— — — 0.2 — — — 0.2 
Balance at June 30, 2020541,545,308 $6.1 $8,673.2 $6,091.5 24,598,074 $(999.7)$(2,024.9)$11,746.2 
__________________
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
 Common StockTreasury Stock
 SharesCostSharesCost
Balance at March 31, 20211,208,530,970 $12.1 $18,464.6 $4,323.6 — $— $(1,385.6)$21,414.7 
Net loss— — — (279.2)— — — (279.2)
Other comprehensive earnings, net of tax— — — — — — 180.6 180.6 
Issuance of restricted stock and stock options exercised, net681,368 — — — — — — — 
Taxes related to the net share settlement of equity awards— — (5.7)— — — — (5.7)
Share-based compensation expense— — 31.0 — — — — 31.0 
Cash dividends declared, $0.11 per common share— — — (134.5)— — — (134.5)
Balance at June 30, 20211,209,212,338 $12.1 $18,489.9 $3,909.9 — $— $(1,205.0)$21,206.9 
Additional Paid-In CapitalRetained
Earnings
Accumulated Other Comprehensive LossTotal
Equity
Common StockTreasury Stock
SharesCostSharesCost
Balance at December 31, 20201,206,895,644 $12.1 $18,438.8 $5,361.2 — $— $(858.0)$22,954.1 
Net loss— — — (1,316.8)— — — (1,316.8)
Other comprehensive loss, net of tax— — — — — — (347.0)(347.0)
Issuance of restricted stock and stock options exercised, net2,316,694 — — — — — — — 
Taxes related to the net share settlement of equity awards— — (12.6)— — — — (12.6)
Share-based compensation expense— — 63.7 — — — — 63.7 
Cash dividends declared, $0.11 per common share— — — (134.5)— — — (134.5)
Balance at June 30, 20211,209,212,338 $12.1 $18,489.9 $3,909.9 — $— $(1,205.0)$21,206.9 
(1)
Ordinary Shares prior to November 16, 2020.

See Notes to Condensed Consolidated Financial Statements
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VIATRIS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Cash Flows
(Unaudited; in millions)
Six Months Ended
June 30,
 20212020
Cash flows from operating activities:
Net (loss) earnings$(1,316.8)$60.2 
Adjustments to reconcile net (loss) earnings to net cash provided by operating activities:
Depreciation and amortization2,739.6 830.7 
Share-based compensation expense63.7 34.7 
Deferred income tax expense (benefit)581.6 (119.7)
Loss from equity method investments34.6 34.5 
Other non-cash items203.5 97.4 
Litigation settlements and other contingencies, net42.4 26.6 
Changes in operating assets and liabilities:
Accounts receivable(114.7)122.6 
Inventories(341.0)(275.8)
Accounts payable(53.5)(234.5)
Income taxes(337.7)49.3 
Other operating assets and liabilities, net(93.5)44.6 
Net cash provided by operating activities1,408.2 670.6 
Cash flows from investing activities:
Cash received from acquisitions277.0 
Capital expenditures(138.8)(87.9)
Purchase of marketable securities(19.5)(90.2)
Proceeds from the sale of marketable securities19.2 33.1 
Payments for product rights and other, net(17.3)(76.4)
Proceeds from sale of assets and subsidiaries83.4 
Proceeds from sale of property, plant and equipment15.5 1.3 
Net cash provided by (used in) investing activities219.5 (220.1)
Cash flows from financing activities:
Proceeds from issuance of long-term debt900.1 33.2 
Payments of long-term debt(2,250.7)(589.0)
Change in short-term borrowings, net199.7 
Cash dividends paid(133.0)
Taxes paid related to net share settlement of equity awards(13.5)(7.1)
Non-contingent payments for product rights(456.0)
Contingent consideration payments(28.6)(43.6)
Payments of financing fees(0.2)(1.2)
Proceeds from exercise of stock options0.6 
Other items, net(3.1)(2.0)
Net cash used in financing activities(1,785.3)(609.1)
Effect on cash of changes in exchange rates(13.3)(7.8)
Net decrease in cash, cash equivalents and restricted cash(170.9)(166.4)
Cash, cash equivalents and restricted cash — beginning of period850.0 491.1 
Cash, cash equivalents and restricted cash — end of period$679.1 $324.7 
Six Months Ended
June 30,
 20222021
Cash flows from operating activities:
Net earnings (loss)$713.1 $(1,316.8)
Adjustments to reconcile net earnings (loss) to net cash provided by operating activities:
Depreciation and amortization1,458.3 2,739.6 
Share-based compensation expense57.7 63.7 
Deferred income tax (benefit) expense(157.6)581.6 
Loss from equity method investments— 34.6 
Other non-cash items3.8 203.5 
Litigation settlements and other contingencies, net10.0 42.4 
Changes in operating assets and liabilities:
Accounts receivable(142.3)(114.7)
Inventories(270.1)(341.0)
Accounts payable254.5 (53.5)
Income taxes17.8 (337.7)
Other operating assets and liabilities, net(4.2)(93.5)
Net cash provided by operating activities1,941.0 1,408.2 
Cash flows from investing activities:
Cash received from acquisitions— 277.0 
Capital expenditures(148.4)(138.8)
Purchase of marketable securities(13.2)(19.5)
Proceeds from the sale of marketable securities12.8 19.2 
Payments for product rights and other, net(13.0)(17.3)
Proceeds from sale of assets and subsidiaries— 83.4 
Proceeds from sale of property, plant and equipment12.8 15.5 
Net cash (used in) provided by investing activities(149.0)219.5 
Cash flows from financing activities:
Proceeds from issuance of long-term debt795.4 900.1 
Payments of long-term debt(1,787.0)(2,250.7)
Change in short-term borrowings, net(473.5)199.7 
Taxes paid related to net share settlement of equity awards(13.2)(13.5)
Non-contingent payments for product rights— (456.0)
Contingent consideration payments(18.9)(28.6)
Payments of financing fees(1.3)(0.2)
Cash dividends paid(290.6)(133.0)
Issuance of common stock0.7 — 
Other items, net(0.2)(3.1)
Net cash used in financing activities(1,788.6)(1,785.3)
Effect on cash of changes in exchange rates(40.2)(13.3)
Net decrease in cash, cash equivalents and restricted cash(36.8)(170.9)
Cash, cash equivalents and restricted cash — beginning of period706.2 850.0 
Cash, cash equivalents and restricted cash — end of period$669.4 $679.1 
See Notes to Condensed Consolidated Financial Statements
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited)

1.General
The accompanying unaudited condensed consolidated financial statements (“interim financial statements”) of Viatris Inc. and subsidiaries were prepared in accordance with U.S. GAAP and the rules and regulations of 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, equity and cash flows for the periods presented.
These interim financial statements should be read in conjunction with the consolidated financial statements and notes thereto in Viatris’ 20202021 Form 10-K. The December 31, 20202021 condensed consolidated balance sheet was derived from audited financial statements.
Turkey Highly Inflationary - Under ASC 830, Foreign Currency Matters (“ASC 830”), a highly inflationary economy is one that has cumulative inflation of approximately 100% or more over a three-year period. Effective April 1, 2022, we classified Turkey as highly inflationary. In accordance with ASC 805, Business Combinations, Mylan is considered830, starting with the accounting acquirersecond quarter of 2022, we began to utilize the Upjohn BusinessU.S. dollar as our functional currency in Turkey, which historically utilized the Turkish lira as the functional currency. The impact of applying the guidance in ASC 830 did not have a material impact on our results of operations, comprehensive earnings, financial position, equity and all historical financial informationcash flows for the three months ended June 30, 2022. The impacted net sales for the three months ended June 30, 2022 and total assets at June 30, 2022 represented less than 1% of the Company prior to November 16, 2020 represents Mylan’s historical resultsour consolidated net sales and the Company’s thereafter. Refer to Note 4 Acquisitions and Other Transactions for additional information.total assets, respectively.
The interim results of operations and comprehensive earnings (loss) for the three and six months ended June 30, 2021,2022, and cash flows for the six months ended June 30, 2021,2022, 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 revenuerevenues in accordance with ASC 606, Revenue from Contracts with Customers. Under ASC 606, the Company recognizes net revenue for product sales when control of the promised goods or services is transferred to our customers in an amount that reflects the consideration we expect to be entitled to in exchange for those goods or services. Revenues are recorded net of provisions for variable consideration, including discounts, rebates, governmental rebate programs, price adjustments, returns, chargebacks, promotional programs and other sales allowances. Accruals for these provisions are presented in the condensed consolidated financial statements as reductions in determining net sales and as a contra asset in accounts receivable, net (if settled via credit) and other current liabilities (if paid in cash).
Our net sales may be impacted by wholesaler and distributor inventory levels of our products, which can fluctuate throughout the year due to the seasonality of certain products, pricing, the timing of product demand, purchasing decisions and other factors. Such fluctuations may impact the comparability of our net sales between periods.
Consideration received from licenses of intellectual property is recorded as other revenues. Royalty or profit share amounts, which are based on sales of licensed products or technology, are recorded when the customer’s subsequent sales or usages occur. Such consideration is included in other revenuerevenues in the condensed consolidated statements of operations.
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
The following table presents the Company’s net sales by product category for each of our reportable segments for the three and six months ended June 30, 20212022 and 2020,2021, respectively:

(In millions)(In millions)Three Months Ended June 30, 2021(In millions)Three Months Ended June 30, 2022
Product CategoryProduct CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotalProduct CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
BrandsBrands$1,424.1 $549.2 $295.4 $433.0 $2,701.7 Brands$1,305.4 $546.3 $243.1 $388.3 $2,483.1 
Complex Gx and BiosimilarsComplex Gx and Biosimilars309.3 9.8 13.7 332.8 Complex Gx and Biosimilars327.0 0.3 12.1 15.4 354.8 
GenericsGenerics907.0 1.1 195.8 423.3 1,527.2 Generics846.7 1.7 171.9 247.2 1,267.5 
TotalTotal$2,640.4 $550.3 $501.0 $870.0 $4,561.7 Total$2,479.1 $548.3 $427.1 $650.9 $4,105.4 

(In millions)Six Months Ended June 30, 2022
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$2,604.1 $1,116.0 $492.1 $825.0 $5,037.2 
Complex Gx and Biosimilars691.1 0.3 22.4 31.8 745.6 
Generics1,660.0 5.1 336.4 499.3 2,500.8 
Total$4,955.2 $1,121.4 $850.9 $1,356.1 $8,283.6 

(In millions)Three Months Ended June 30, 2021
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$1,424.1 $549.2 $295.4 $433.0 $2,701.7 
Complex Gx and Biosimilars309.3 — 9.8 13.7 332.8 
Generics907.0 1.1 195.8 423.3 1,527.2 
Total$2,640.4 $550.3 $501.0 $870.0 $4,561.7 

(In millions)Six Months Ended June 30, 2021
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$2,827.8 $1,140.1 $579.4 $879.0 $5,426.3 
Complex Gx and Biosimilars621.3 — 18.7 21.7 661.7 
Generics1,762.9 2.1 384.8 724.0 2,873.8 
Total$5,212.0 $1,142.2 $982.9 $1,624.7 $8,961.8 

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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
(In millions)Six Months Ended June 30, 2021
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$2,827.8 $1,140.1 $579.4 $879.0 $5,426.3 
Complex Gx and Biosimilars621.3 18.7 21.7 661.7 
Generics1,762.9 2.1 384.8 724.0 2,873.8 
Total$5,212.0 $1,142.2 $982.9 $1,624.7 $8,961.8 

(In millions)Three Months Ended June 30, 2020
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$855.5 $22.0 $128.1 $67.4 $1,073.0 
Complex Gx and Biosimilars328.6 8.5 14.0 351.1 
Generics798.6 0.7 143.6 328.9 1,271.8 
Total$1,982.7 $22.7 $280.2 $410.3 $2,695.9 

(In millions)Six Months Ended June 30, 2020
Product CategoryDeveloped MarketsGreater ChinaJANZEmerging MarketsTotal
Brands$1,747.0 $36.7 $218.7 $132.1 $2,134.5 
Complex Gx and Biosimilars570.2 0.1 16.9 17.2 604.4 
Generics1,651.9 1.0 287.8 604.5 2,545.2 
Total$3,969.1 $37.8 $523.4 $753.8 $5,284.1 
The following table presents net sales on a consolidated basis for select key products for the three and six months ended June 30, 2022 and 2021:
Three months ended June 30,Six months ended June 30,
(In millions)(In millions)Three months ended June 30, 2021Six months ended June 30, 2021(In millions)2022202120222021
Select Key Global ProductsSelect Key Global ProductsSelect Key Global Products
Lipitor ®Lipitor ®$398.3 $862.9 Lipitor ®$405.6 $398.3 $845.7 $862.9 
Norvasc ®Norvasc ®209.8 437.5 Norvasc ®203.0 209.8 410.8 437.5 
Lyrica ®Lyrica ®192.5 380.3 Lyrica ®155.8 192.5 327.4 380.3 
Viagra ®Viagra ®134.8 274.4 Viagra ®115.1 134.8 244.9 274.4 
EpiPen® Auto-InjectorsEpiPen® Auto-Injectors104.1 207.8 EpiPen® Auto-Injectors106.5 104.1 195.3 207.8 
Effexor ®83.5 160.1 
Celebrex ®Celebrex ®82.3 171.3 Celebrex ®85.9 82.3 171.2 171.3 
Creon ®Creon ®80.7 150.6 Creon ®75.4 80.7 150.1 150.6 
Effexor ®Effexor ®73.7 83.5 151.2 160.1 
Zoloft ®Zoloft ®70.9 147.5 Zoloft ®62.5 70.9 135.6 147.5 
XalabrandsXalabrands58.3 116.2 Xalabrands42.7 58.3 95.7 116.2 
Select Key Segment ProductsSelect Key Segment ProductsSelect Key Segment Products
Dymista ®Dymista ®$54.6 $94.9 Dymista ®$55.5 $54.6 $99.4 $94.9 
Yupelri ®Yupelri ®49.1 41.8 92.7 78.7 
Amitiza ®Amitiza ®52.1 98.0 Amitiza ®44.1 52.1 85.9 98.0 
Xanax ®Xanax ®48.8 93.9 Xanax ®37.2 48.8 77.2 93.9 
Yupelri ®41.8 78.7 
____________
(a)The Company does not disclose net sales for any products considered competitively sensitive.
(b)Products disclosed may change in future periods, including as a result of seasonality, competition or new product introductions.launches.
13

Table(c)Amounts for the three and six months ended June 30, 2022 include the unfavorable impact of Contentsforeign currency translations compared to the prior year period.
VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Variable Consideration and Accounts Receivable
The following table presents a reconciliation of gross sales to net sales by each significant category of variable consideration during the three and six months ended June 30, 20212022 and 2020,2021, respectively:
Three Months EndedSix Months EndedThree Months EndedSix Months Ended
June 30,June 30,June 30,June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
Gross salesGross sales$7,752.3 $4,457.6 $15,319.3 $8,881.6 Gross sales$7,008.7 $7,752.3 $14,207.0 $15,319.3 
Gross to net adjustments:Gross to net adjustments:Gross to net adjustments:
ChargebacksChargebacks(1,354.8)(795.5)(2,672.8)(1,649.9)Chargebacks(1,594.2)(1,354.8)(3,178.4)(2,672.8)
Rebates, promotional programs and other sales allowancesRebates, promotional programs and other sales allowances(1,566.6)(820.4)(3,135.1)(1,666.0)Rebates, promotional programs and other sales allowances(1,075.3)(1,566.6)(2,281.2)(3,135.1)
ReturnsReturns(88.3)(57.6)(201.3)(116.6)Returns(82.7)(88.3)(165.3)(201.3)
Governmental rebate programsGovernmental rebate programs(180.9)(88.2)(348.3)(165.0)Governmental rebate programs(151.1)(180.9)(298.5)(348.3)
Total gross to net adjustmentsTotal gross to net adjustments$(3,190.6)$(1,761.7)$(6,357.5)$(3,597.5)Total gross to net adjustments$(2,903.3)$(3,190.6)$(5,923.4)$(6,357.5)
Net salesNet sales$4,561.7 $2,695.9 $8,961.8 $5,284.1 Net sales$4,105.4 $4,561.7 $8,283.6 $8,961.8 
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
No significant revisions were made to the methodology used in determining these provisions or the nature of the provisions during the three and six months ended June 30, 2021.2022. Such allowances were comprised of the following at June 30, 20212022 and December 31, 2020,2021, respectively:
(In millions)(In millions)June 30,
2021
December 31,
2020
(In millions)June 30,
2022
December 31,
2021
Accounts receivable, netAccounts receivable, net$1,667.9 $1,802.9 Accounts receivable, net$1,742.9 $1,688.6 
Other current liabilitiesOther current liabilities1,083.6 1,211.8 Other current liabilities914.7 1,362.1 
TotalTotal$2,751.5 $3,014.7 Total$2,657.6 $3,050.7 
Accounts receivable, net was comprised of the following at June 30, 20212022 and December 31, 2020,2021, respectively:
(In millions)(In millions)June 30,
2021
December 31,
2020
(In millions)June 30,
2022
December 31,
2021
Trade receivables, netTrade receivables, net$3,880.4 $3,891.3 Trade receivables, net$3,182.9 $3,774.4 
Other receivablesOther receivables598.3 952.5 Other receivables553.3 492.0 
Accounts receivable, netAccounts receivable, net$4,478.7 $4,843.8 Accounts receivable, net$3,736.2 $4,266.4 
Accounts Receivable Factoring Arrangements
We have entered into accounts receivable factoring agreements with financial institutions to sell certain of our non-U.S. accounts receivable. These transactions are accounted for as sales and result in a reduction in accounts receivable because the agreements transfer effective control over and risk related to the receivables to the buyers. Our factoring agreements do not allow for recourse in the event of uncollectibility, and we do not retain any interest in the underlying accounts receivable once sold. We derecognized $112.9$41.9 million and $153.0$29.6 million of accounts receivable as of June 30, 20212022 and December 31, 2020,2021, respectively, under these factoring arrangements.



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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
3.Recent Accounting Pronouncements
Adoption of New Accounting StandardsStandard
In January 2020,November 2021, the FASB issued Accounting Standards Update 2020-01,2021-10, Clarifying the Interactions Between Topic 321, Topic 323, and Topic 815 (“ASU 2020-01”),Government Assistance (Topic 832): Disclosures by Business Entities about Government Assistance (“ASU 2021-10”), which clarifiesrequires entities to provide annual disclosures about transactions with a government that an entity should consider observable transactions that require it to either apply or discontinue the equity method of accounting for the purposes of applying the measurement alternative in accordance with Topic 321 immediately before applying or upon discontinuing the equity method. In addition, ASU 2020-01 states that for the purpose of applying paragraph 815-10-15-141(a) an entity should not consider whether, upon the settlement of the forward contract or exercise of the purchased option, individually or with existing investments, the underlying securities would beare accounted for underby applying a grant or contribution accounting model by analogy. We adopted the equity method in Topic 323 or the fair value option in accordance with the financial instruments guidance in Topic 825. ASU 2020-01 was effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2020.prospectively on January 1, 2022. The adoption of this guidance didadditional annual disclosures required are not expected to have a material impact on the Company’s condensedour consolidated financial statements and disclosures.statements.
In December 2019, the FASB issued Accounting Standards Update 2019-12, Income Taxes (Topic 740) which is intended to simplify theThere were no other significant changes in new accounting for income taxes by eliminating certain exceptions and simplifying certain requirements under Topic 740. ASU 2019-12 was effective for fiscal years, and interim periods withinstandards from those fiscal years, beginning after December 15, 2020. ASU 2019-12 includes an update to previous guidancedisclosed in situations in which an entity incurs a loss on a year-to-date basis that exceeds the anticipated loss for the year. In these situations, previous guidance stipulated that the income tax benefit was limited to the income tax that would exist on the basis of the year-to-date loss. This represented an exception to the guidance in ASC 740-270, and the provisions of ASU 2019-12 include the elimination of this exception which applied to the financial results of the three and six months ended June 30, 2021. The Company has applied the provisions of ASU 2019-12 on a prospective basis beginning January 1, 2021. The adoption of this guidance did not have a material impact on the Company’s condensed consolidated financial statements and disclosures.
Accounting Standard Issued Not Yet Adopted
The following recently issued accounting standard has not been adopted.Viatris’ 2021 Form 10-K. Refer to Viatris’ 20202021 Form 10-K for additional information and its potential impacts.
Accounting Standard UpdateEffective Date
ASU 2020-04: Reference Rate Reform (Topic 848) Facilitation of the Effects of Reference Rate Reform on Financial Reporting
January 1, 2023
information.
4.Acquisitions and Other Transactions
Upjohn Business Combination Agreement
On July 29, 2019, Mylan, Pfizer, Upjohn Inc., a wholly-owned subsidiary of Pfizer, and certain other affiliated entities entered into a Business Combination Agreement pursuant to which Mylan would combine with the Upjohn Business in a Reverse Morris Trust transaction. The Upjohn Business was a global, primarily off-patent branded and generic established medicines business, which includes 20 primarily off-patent solid oral dose legacy brands, such as Lyrica, Lipitor, Celebrex and Viagra. The Combination was completed on November 16, 2020.
Prior to the Combination and pursuant to a Separation and Distribution Agreement, Pfizer had, among other things, transferred to Viatris substantially all of the assets and liabilities comprising the Upjohn Business (the Separation) and, thereafter, Pfizer had distributed to Pfizer stockholders all of the issued and outstanding shares of Viatris (the Distribution). When the Distribution and Combination were complete, Pfizer stockholders as of the record date of the Distribution owned 57% of the outstanding shares of Viatris common stock and Mylan shareholders as of immediately before the Combination owned 43% of the outstanding shares of Viatris common stock, in each case on a fully diluted basis. Viatris also made a cash payment to Pfizer equal to $12 billion, which was funded with the proceeds of debt incurred by Upjohn prior to the Combination.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
The transaction involved multiple legal entity restructuring transactionsand a reverse merger acquisition with Viatris representing the legal acquirer and Mylan representing the accounting acquirer of the Upjohn Business. In accordance with ASC 805, Business Combinations, Mylan is considered the accounting acquirer of the Upjohn Business and Viatris applied purchase accounting to the acquired assets and assumed liabilities of the Upjohn Business as of November 16, 2020. The debt incurred by Upjohn prior to the Combination was a liability assumed in purchase accounting. The fair value of the debt as of November 16, 2020 was $13.08 billion.
The purchase price consists of the issuance of approximately 689.9 million Viatris shares of common stock at a fair value of approximately $10.73 billion based on the closing price of Mylan’s ordinary shares on November 13, 2020, as reported by the NASDAQ. 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 $602.9 million were incurred during the twelve months ended December 31, 2020, and approximately $108.2 million were incurred during the six months ended June 30, 2021. Acquisition related costs were recorded primarily in SG&A in the consolidated statements of operations for such periods.
During the six months ended June 30, 2021, adjustments were made to the preliminary purchase price recorded at November 16, 2020. These adjustments are reflected in the values presented below. The preliminary allocation of the $10.73 billion purchase price to the assets acquired and liabilities assumed under the Combination is as follows:
(In millions)
Preliminary Purchase Price Allocation as of December 31, 2020 (a)
Measurement Period and Other Adjustments (b)
Preliminary Purchase Price Allocation as of June 30, 2021 (as adjusted)
Current assets (excluding inventories and net of cash acquired)$2,841.9 $(10.6)$2,831.3 
Inventories2,588.9 (34.2)2,554.7 
Property, plant and equipment1,394.1 — 1,394.1 
Identified intangible assets18,040.0 — 18,040.0 
Goodwill2,107.5 (134.7)1,972.8 
Deferred income tax benefit1,481.9 244.0 1,725.9 
Other assets792.1 — 792.1 
Total assets acquired$29,246.4 $64.5 $29,310.9 
Current liabilities2,760.2 64.4 2,824.6 
Long-term debt, including current portion13,076.2 — 13,076.2 
Deferred tax liabilities1,656.9 — 1,656.9 
Other noncurrent liabilities1,441.5 0.1 1,441.6 
Net assets acquired (net of $415.8 of cash acquired)$10,311.6 $$10,311.6 
____________
(a)As previously reported in Viatris’ 2020 Form 10-K.
(b)The measurement period adjustments are primarily for 1) certain working capital adjustments and an increase in litigation reserves to reflect facts and circumstances that existed as of the date of the Combination and 2) the tax implications of these and other adjustments. These adjustments did not have a significant impact on the Company’s previously reported consolidated financial statements and accordingly, the Company has not retrospectively adjusted those consolidated financial statements.
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 components and income taxes.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
During the year ended December 31, 2020, the Company recorded a step-up in the fair value of inventory of approximately $1.43 billion. During the three and six months ended June 30, 2021, the Company recorded amortization of the inventory step-up of approximately $477.3 million and $953.7 million, respectively, which is included in cost of sales in the condensed consolidated statements of operations. In addition, during the year ended December 31, 2020, a step-up in the fair value of property, plant and equipment of approximately $390.0 million was recognized. The related depreciation is being expensed over a service life of five years for machinery and equipment and between 10 and 20 years for buildings.
The identified intangible assets of $18.04 billion are comprised of product rights and are being amortized over a weighted average useful life of 15 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 $1.97 billion arising from the Combination consisted largely of the value of the employee workforce and products to be sold in new markets leveraging the combined entity. In addition, an allocation of the goodwill was assigned to the respective segments. None of the goodwill recognized in this transaction is expected to be deductible for income tax purposes.
The Company recorded a fair value adjustment of approximately $759.4 million related to the long-term debt assumed as part of the acquisition. The fair value of long-term debt as of the Combination date was determined by broker or dealer quotations, which is classified as Level 2 in the fair value hierarchy. The total fair value adjustment is being amortized as a reduction to interest expense over the maturity dates of the related debt instruments.
Unaudited Pro Forma Financial Results
The following table presents supplemental unaudited pro forma information for the Combination, as if it had occurred on January 1, 2019. The unaudited pro forma results reflect certain adjustments related to past operating performance and acquisition accounting adjustments, such as increased depreciation and 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 Combination. 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 date above, nor are they indicative of the future operating results of Viatris and its subsidiaries.
Three Months EndedSix Months Ended
(Unaudited, in millions, except per share amounts)June 30, 2020June 30, 2020
Total revenues$4,555.4 $8,994.8 
Net earnings$681.1 $1,223.7 
Earnings per share:
Basic$0.56 $1.01 
Diluted$0.56 $1.01 
Weighted average shares outstanding:
Basic1,206.9 1,206.6 
Diluted1,207.1 1,207.0 
5.Share-Based Incentive Plan
Prior to the Distribution, Viatris adopted and Pfizer, in the capacity as Viatris’ sole stockholder at such time, approved the Plan which became effective as of the Distribution. In connection with the Combination, as of November 16, 2020, the Company assumed the Mylan N.V. Amended and Restated 2003 Long-Term Incentive Plan,LTIP, which had previously been approved by Mylan shareholders. The Plan and 2003 LTIP include (i) 72,500,000 shares of common stock authorized for grant pursuant to the Plan, which may include dividend payments payable in common stock on unvested shares granted under awards, (ii) 6,757,640 shares of common stock to be issued pursuant to the exercise of outstanding stock options granted to participants under the 2003 LTIP and assumed by Viatris in connection with the Combination and (iii) 13,535,627 shares of common stock subject to outstanding equity-based awards, other than stock options, assumed by Viatris in connection with the Combination, or that otherwise remain available for issuance under the 2003 LTIP.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Under the Plan and 2003 LTIP, 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, SARs, restricted stock and units, PSUs, other stock-based awards and short-term cash awards. Stock option awards are granted with an exercise price equal to the fair market value of the shares underlying the stock options at the date of the grant, generally become exercisable over periods ranging from three to four years, and generally expire in ten years.
The following table summarizes stock optionawards (stock options and SAR (together, “stock awards”)SARs) activity under the Plan and 2003 LTIP:
Number of Shares Under Stock AwardsWeighted Average Exercise Price per Share
Outstanding at December 31, 20206,711,731 $35.36 
Forfeited(938,524)$24.77 
Outstanding at June 30, 20215,773,207 $37.09 
Vested and expected to vest at June 30, 20215,668,426 $37.37 
Exercisable at June 30, 20215,053,633 $39.38 
Number of Shares Under Stock AwardsWeighted Average Exercise Price per Share
Outstanding at December 31, 20215,576,490 $37.19 
Forfeited(782,735)$30.69 
Outstanding at June 30, 20224,793,755 $38.25 
Vested and expected to vest at June 30, 20224,748,296 $38.43 
Exercisable at June 30, 20224,518,196 $39.43 
As of June 30, 2021,2022, stock awards outstanding, stock awards vested and expected to vest and stock awards exercisable had average remaining contractual terms of 5.14.5 years, 5.14.5 years and 4.74.3 years, respectively. Also, atas of June 30, 2021,2022, stock awards outstanding, stock awards vested and expected to vest and stock awards exercisable had 0no aggregate intrinsic value.
A summary of the status of the Company’s nonvested restricted stock awards (restricted stock and restricted stock unit awards, including PSUs) as of June 30, 20212022 and the changes during the six months ended June 30, 20212022 are presented below:
Number of Restricted Stock AwardsWeighted Average Grant-Date Fair Value Per ShareNumber of Restricted Stock AwardsWeighted Average Grant-Date Fair Value Per Share
Nonvested at December 31, 202012,073,790 $18.34 
Nonvested at December 31, 2021Nonvested at December 31, 202116,858,128 $15.12 
GrantedGranted9,731,270 14.28 Granted16,778,913 10.20 
ReleasedReleased(2,824,976)25.47 Released(3,576,289)17.92 
ForfeitedForfeited(890,764)15.69 Forfeited(730,250)12.85 
Nonvested at June 30, 202118,089,320 $15.17 
Nonvested at June 30, 2022Nonvested at June 30, 202229,330,502 $12.01 
As of June 30, 2021,2022, the Company had $201.9$238.6 million of total unrecognized compensation expense, net of estimated forfeitures, related to all of its stock-based awards, which we expect to recognize over the remaining weighted average vesting period of 2.01.8 years. The total intrinsic value of stock awards exercised and restricted stock units released during the six months ended June 30, 2022 and 2021 and 2020 was $71.9$64.1 million and $19.1$71.9 million, respectively.
6.5.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. Employees in the U.S., Puerto Rico and certain international locations are also provided retirement benefits through defined contribution plans.
The Company also sponsors other postretirement benefit plans including plans that provide for postretirement supplemental medical coverage. Benefits from these plans are provided to employees and their spouses and dependents who meet various minimum age and service requirements. In addition, the Company sponsors other plans that provide for life insurance benefits and postretirement medical coverage for certain officers and management employees.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
In connection with the Combination, the Company assumed certain post retirement defined benefit pension plans sponsored by Upjohn. The most significant plans include those in Puerto Rico, Ireland and Japan. Upjohn is also the sponsor of one postretirement medical plan in Puerto Rico. As part of the acquisition accounting, the Company has recorded the fair value of these plans using assumptions and accounting policies consistent with those historically utilized by Mylan. Upon completion of the Combination, the excess of projected benefit obligation over the plan assets was recognized as a liability and any existing unrecognized actuarial gains or losses and unrecognized service costs or benefits were eliminated in purchase accounting.
Net Periodic Benefit Cost
Components of net periodic benefit cost for the three and six months ended June 30, 20212022 and 20202021 were as follows:
Pension and Other Postretirement BenefitsPension and Other Postretirement Benefits
Three Months EndedSix Months EndedThree Months EndedSix Months Ended
June 30,June 30,June 30,June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
Service costService cost$10.9 $5.3 $21.7 $10.6 Service cost$9.5 $10.9 $19.0 $21.7 
Interest costInterest cost8.7 2.9 17.2 5.8 Interest cost10.4 8.7 20.8 17.2 
Expected return on plan assetsExpected return on plan assets(16.7)(3.4)(33.2)(6.8)Expected return on plan assets(16.6)(16.7)(33.2)(33.2)
Amortization of prior service costsAmortization of prior service costs(0.2)(0.3)Amortization of prior service costs— (0.2)0.1 (0.3)
Recognized net actuarial lossesRecognized net actuarial losses0.5 0.1 0.8 0.3 Recognized net actuarial losses0.1 0.5 0.1 0.8 
Settlement gainSettlement gain(3.1)(3.1)Settlement gain$— $(3.1)$— $(3.1)
Net periodic benefit costNet periodic benefit cost$0.1 $4.9 $3.1 $9.9 Net periodic benefit cost$3.4 $0.1 $6.8 $3.1 
In the second quarter of 2021, the Company recognized a settlement gain as a result of cash payments from lump sum elections related to the U.S. and Puerto Rico pension plans.
The Company is making the minimum mandatory contributions to its defined benefit pension plans in the U.S. and Puerto Rico for the 2022 plan year. The Company expects to make total benefit payments of approximately $118.9$118.0 million from pension and other postretirement benefit plans in 2021.2022. The Company anticipates making contributions to pension and other postretirement benefit plans of approximately $70.1$52.0 million in 2021 due to the second quarter remeasurement of the impacted plans.2022.
7.6.Balance Sheet Components
Selected balance sheet components consist of the following:
Cash and restricted cash
(In millions)(In millions)June 30,
2021
December 31,
2020
June 30, 2020(In millions)June 30,
2022
December 31,
2021
June 30, 2021
Cash and cash equivalentsCash and cash equivalents$673.9 $844.4 $323.6 Cash and cash equivalents$664.7 $701.2 $673.9 
Restricted cash, included in other current and non-current assets5.2 5.6 1.1 
Restricted cash, included in prepaid expenses and other current assetsRestricted cash, included in prepaid expenses and other current assets4.7 5.0 5.2 
Cash, cash equivalents and restricted cashCash, cash equivalents and restricted cash$679.1 $850.0 $324.7 Cash, cash equivalents and restricted cash$669.4 $706.2 $679.1 
Inventories
(In millions)(In millions)June 30,
2021
December 31,
2020
(In millions)June 30,
2022
December 31,
2021
Raw materialsRaw materials$948.2 $958.4 Raw materials$805.2 $922.4 
Work in processWork in process1,148.6 1,438.1 Work in process821.7 993.3 
Finished goodsFinished goods2,390.8 3,075.4 Finished goods1,985.6 2,062.0 
InventoriesInventories$4,487.6 $5,471.9 Inventories$3,612.5 $3,977.7 
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Prepaid expenses and other current assets
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Prepaid expensesPrepaid expenses$221.6 $267.8 Prepaid expenses$274.0 $256.7 
Available-for-sale fixed income securitiesAvailable-for-sale fixed income securities38.5 39.1 Available-for-sale fixed income securities35.5 38.2 
Fair value of financial instrumentsFair value of financial instruments90.3 118.6 Fair value of financial instruments201.1 144.6 
Equity securitiesEquity securities49.6 45.8 Equity securities41.7 51.0 
Other current assetsOther current assets1,709.6 1,236.1 Other current assets1,145.4 1,467.1 
Prepaid expenses and other current assetsPrepaid expenses and other current assets$2,109.6 $1,707.4 Prepaid expenses and other current assets$1,697.7 $1,957.6 
Prepaid expenses consist primarily of prepaid rent, insurance and other individually insignificant items.
Property, plant and equipment, net
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Machinery and equipmentMachinery and equipment$3,191.2 $3,235.0 Machinery and equipment$2,820.9 $3,054.0 
Buildings and improvementsBuildings and improvements1,916.2 1,954.8 Buildings and improvements1,548.1 1,808.5 
Construction in progressConstruction in progress403.7 376.3 Construction in progress551.7 588.7 
Land and improvementsLand and improvements152.0 155.8 Land and improvements120.7 137.9 
Gross property, plant and equipmentGross property, plant and equipment5,663.1 5,721.9 Gross property, plant and equipment5,041.4 5,589.1 
Accumulated depreciationAccumulated depreciation2,491.7 2,262.0 Accumulated depreciation1,957.5 2,400.5 
Property, plant and equipment, netProperty, plant and equipment, net$3,171.4 $3,459.9 Property, plant and equipment, net$3,083.9 $3,188.6 
Other assets
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Equity method investments, clean energy investments$24.2 $47.9 
Operating lease right-of-use assetsOperating lease right-of-use assets300.6 323.6 Operating lease right-of-use assets$275.1 $290.8 
Other long-term assetsOther long-term assets700.3 676.0 Other long-term assets722.3 879.9 
Other assetsOther assets$1,025.1 $1,047.5 Other assets$997.4 $1,170.7 
Accounts payable
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Trade accounts payableTrade accounts payable$1,319.5 $1,345.7 Trade accounts payable$1,050.7 $1,056.1 
Other payablesOther payables480.7 558.5 Other payables619.4 601.3 
Accounts payableAccounts payable$1,800.2 $1,904.2 Accounts payable$1,670.1 $1,657.4 
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Other current liabilities
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Accrued sales allowancesAccrued sales allowances$1,083.6 $1,211.8 Accrued sales allowances$914.7 $1,362.1 
Legal and professional accruals, including litigation accrualsLegal and professional accruals, including litigation accruals487.7 362.9 Legal and professional accruals, including litigation accruals676.3 715.6 
Payroll and employee benefit liabilitiesPayroll and employee benefit liabilities663.2 828.2 Payroll and employee benefit liabilities541.0 741.9 
Contingent considerationContingent consideration83.1 100.5 Contingent consideration73.8 66.7 
Accrued restructuringAccrued restructuring136.3 233.5 
Accrued interestAccrued interest81.5 90.9 Accrued interest75.7 86.6 
Restructuring372.9 149.2 
Equity method investments, clean energy investmentsEquity method investments, clean energy investments29.1 47.5 Equity method investments, clean energy investments4.3 10.9 
Fair value of financial instrumentsFair value of financial instruments40.1 103.6 Fair value of financial instruments101.9 61.0 
Operating lease liabilityOperating lease liability89.5 92.9 Operating lease liability83.4 86.7 
OtherOther1,280.8 1,973.2 Other1,205.0 1,254.6 
Other current liabilitiesOther current liabilities$4,211.5 $4,960.7 Other current liabilities$3,812.4 $4,619.6 
Other long-term obligations
(In millions)(In millions)June 30,
2021
December 31, 2020(In millions)June 30,
2022
December 31, 2021
Employee benefit liabilitiesEmployee benefit liabilities$912.4 $1,020.4 Employee benefit liabilities$832.6 $876.4 
Contingent considerationContingent consideration130.7 123.1 Contingent consideration107.2 133.0 
Tax related items, including contingenciesTax related items, including contingencies389.3 469.5 Tax related items, including contingencies411.3 426.1 
Operating lease liabilityOperating lease liability208.6 229.5 Operating lease liability192.2 200.9 
Accrued Restructuring126.6 134.8 
Accrued restructuringAccrued restructuring51.2 64.3 
OtherOther474.3 505.8 Other219.7 232.9 
Other long-term obligationsOther long-term obligations$2,241.9 $2,483.1 Other long-term obligations$1,814.2 $1,933.6 
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Assets and liabilities held for sale
On February 27, 2022, the Company entered into an agreement to contribute its biosimilars portfolio to Biocon Biologics. Under the terms of the Biocon Agreement, at closing Viatris will receive an up-front cash payment of $2.0 billion, subject to certain adjustments, ownership of at least 12.9% of Biocon Biologics, on a fully diluted basis, in the form of convertible preferred equity which will have certain priority rights with respect to certain liquidity events, and $335 million as additional cash payments that are expected to be paid in 2024. Upon closing of the transaction, we expect to record a gain for the difference between the consideration received, including the fair value of the convertible preferred equity, and the carrying value of the biosimilars portfolio. The companies will also enter into a two-year transition services agreement, subject to extension in certain circumstances, during which time Viatris will provide certain commercial and administrative services for an applicable service fee. The transaction is expected to close in the second half of 2022 and is subject to various closing conditions (including regulatory approvals). Assets and liabilities associated with the biosimilars portfolio were reclassified as held for sale in the condensed consolidated balance sheets as of June 30, 2022.

The amounts associated with the biosimilars portfolio, as well as other assets classified as held for sale, consisted of the following:

As of
(In millions)June 30, 2022
Assets held for sale
Accounts receivable, net$179.1 
Inventories168.5 
Prepaid expenses and other current assets15.4 
Intangible assets, net59.9 
Goodwill936.9 
Other assets105.6 
Total assets held for sale$1,465.4 
Liabilities held for sale
Accounts payable$112.9 
Other current liabilities172.2 
Total liabilities held for sale$285.1 

For the three and six months ended June 30, 2022, total revenues relating to the biosimilars portfolio expected to be contributed to Biocon Biologics were approximately $166.9 million and $336.0 million, respectively.
8.7.Equity Method Investments
The law that provides for IRC Section 45 tax credits expired during the year ended December 31, 2021 for all three clean energy investments and all of the clean energy investments have wound down operations. Summarized financial information, in the aggregate, for the Company’s 3 equity method, clean energy investments on a 100% basis for the three and six months ended June 30, 2021 and 2020 are as follows:
Three Months EndedSix Months EndedThree Months EndedSix Months Ended
June 30,June 30,
(In millions)(In millions)2021202020212020(In millions)June 30, 2021June 30, 2021
Total revenuesTotal revenues$90.0 $87.8 $199.5 $175.3 Total revenues$90.0 $199.5 
Gross lossGross loss(1.2)(1.1)(2.6)(2.2)Gross loss(1.2)(2.6)
Operating and non-operating expenseOperating and non-operating expense4.0 4.5 8.9 9.2 Operating and non-operating expense4.0 8.9 
Net lossNet loss$(5.2)$(5.6)$(11.5)$(11.4)Net loss$(5.2)$(11.5)
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
The Company’s net losses from its equity method investments includeincluded amortization expense related to the excess of the cost basis of the Company’s investment over the underlying assets of each individual investee. For the three and six months ended June 30, 2021, and 2020, the Company recognized net losses from equity method investments of $16.7 million and $17.2 million, respectively. For the six months ended June 30, 2021 and 2020, the Company recognized net losses from equity method investments of $34.6 million and $34.5 million, respectively, which were recognized as a component of other expense, net in the condensed consolidated statements of operations. The Company recognizesrecognized the income tax credits and benefits from the clean energy investments as part of its provision for income taxes.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
9.8.Earnings (Loss) Earnings per Share
Basic earnings (loss) earnings per share is computed by dividing net earnings (loss) earnings by the weighted average number of shares outstanding during the period. Diluted earnings (loss) earnings per share is computed by dividing net earnings (loss) earnings by the weighted average number of shares outstanding during the period increased by the number of additional shares that would have been outstanding related to potentially dilutive securities or instruments, if the impact is dilutive.
Basic and diluted earnings (loss) earnings per share attributable to Viatris Inc. are calculated as follows:
 Three Months EndedSix Months Ended
June 30,June 30,
(In millions, except per share amounts)2021202020212020
Basic (loss) earnings attributable to Viatris Inc. common shareholders
Net (loss) earnings attributable to Viatris Inc. common shareholders$(279.2)$39.4 $(1,316.8)$60.2 
Shares (denominator):
Weighted average shares outstanding1,208.8 516.9 1,208.2 516.7 
Basic (loss) earnings per share attributable to Viatris Inc. shareholders$(0.23)$0.08 $(1.09)$0.12 
Diluted (loss) earnings attributable to Viatris Inc. common shareholders
Net (loss) earnings attributable to Viatris Inc. common shareholders$(279.2)$39.4 $(1,316.8)$60.2 
Shares (denominator):
Weighted average shares outstanding1,208.8 516.9 1,208.2 516.7 
Share-based awards and warrants0.3 0.4 
Total dilutive shares outstanding1,208.8 517.2 1,208.2 517.1 
Diluted (loss) earnings per share attributable to Viatris Inc. shareholders$(0.23)$0.08 $(1.09)$0.12 
 Three Months EndedSix Months Ended
June 30,June 30,
(In millions, except per share amounts)2022202120222021
Basic earnings (loss) attributable to Viatris Inc. common shareholders
Net earnings (loss) attributable to Viatris Inc. common shareholders$313.9 $(279.2)$713.1 $(1,316.8)
Shares (denominator):
Weighted average shares outstanding1,212.3 1,208.8 1,211.4 1,208.2 
Basic earnings (loss) per share attributable to Viatris Inc. shareholders$0.26 $(0.23)$0.59 $(1.09)
Diluted earnings (loss) attributable to Viatris Inc. common shareholders
Net earnings (loss) attributable to Viatris Inc. common shareholders$313.9 $(279.2)$713.1 $(1,316.8)
Shares (denominator):
Weighted average shares outstanding1,212.3 1,208.8 1,211.4 1,208.2 
Share-based awards4.8 — 3.7 — 
Total dilutive shares outstanding1,217.1 1,208.8 1,215.1 1,208.2 
Diluted earnings (loss) per share attributable to Viatris Inc. shareholders$0.26 $(0.23)$0.59 $(1.09)
Additional stock awards and restricted stock awards were outstanding during the three and six months ended June 30, 20212022 and 2020,2021, but were not included in the computation of diluted earnings per share for each respective period because the effect would be anti-dilutive. Excluded shares at June 30, 20212022 include certain share-based compensation awards whose performance conditions had not been fully met. Such excluded shares and anti-dilutive awards represented 9.8 million shares and 12.6 million shares for the three and six months ended June 30, 2022, respectively, and 10.0 million shares and 10.5 million shares for the three and six months ended June 30, 2021, respectively, and 11.1 million shares and 10.4 million shares for the three and six months ended 2020, respectively.
On May 7, 2021, the Company’s BoardThe Company paid quarterly dividends of Directors declared an inaugural quarterly cash dividend of $0.11$0.12 per share on the Company’s issued and outstanding common stock. The first quarterly cash dividend was paidstock on March 16, 2022 and June 16, 2021 to shareholders of record as of the close of business on May 24, 2021.2022. On August 6, 2021,4, 2022, the Company’s Board of Directors declared its seconda quarterly cash dividend of $0.11$0.12 per share on the Company’s issued and outstanding common stock, which will be payable on September 16, 20212022 to shareholders of record as of the close of business on August 24, 2021.2022. The declaration and payment of future dividends to holders of the Company’s common stock will be at the discretion of the Board of Directors, and will depend upon factors, including but not limited to, the Company’s financial condition, earnings, capital requirements of its businesses, legal requirements, regulatory constraints, industry practice, and other factors that the Board of Directors deems relevant.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
On May 6, 2022, the Company announced that its Board of Directors had authorized a DRIP. The DRIP allows shareholders to automatically reinvest all or a portion of the cash dividends paid on their shares of the Company’s common stock and to make certain additional optional cash investments in the Company’s common stock.
10.
On February 28, 2022, the Company announced that its Board of Directors had authorized a share repurchase program for the repurchase of up to $1.0 billion of the Company’s shares of common stock. The Company has not yet repurchased any shares of common stock under the share repurchase program and the share repurchase program does not obligate the Company to acquire any particular amount of common stock.

9.Goodwill and Intangible Assets
Goodwill
The changes in the carrying amount of goodwill for the six months ended June 30, 20212022 are as follows:
(In millions)(In millions)Developed MarketsGreater ChinaJANZEmerging MarketsTotal(In millions)Developed MarketsGreater ChinaJANZEmerging MarketsTotal
Balance at December 31, 2020:
Balance at December 31, 2021:Balance at December 31, 2021:
GoodwillGoodwill$9,569.5 $738.3 $864.0 $1,560.2 $12,732.0 Goodwill$9,108.4 $969.5 $776.3 $1,644.5 $12,498.7 
Accumulated impairment lossesAccumulated impairment losses(385.0)(385.0)Accumulated impairment losses(385.0)— — — (385.0)
9,184.5 738.3 864.0 1,560.2 12,347.0 8,723.4 969.5 776.3 1,644.5 12,113.7 
Measurement period adjustments(45.1)(41.7)(13.9)(34.0)(134.7)
Reclassification to assets held for sale (1)
Reclassification to assets held for sale (1)
(746.0)(2.8)(33.2)(154.9)(936.9)
Foreign currency translationForeign currency translation(251.1)6.6 (35.9)58.5 (221.9)Foreign currency translation(525.5)(14.8)(53.8)(59.7)(653.8)
$8,888.3 $703.2 $814.2 $1,584.7 $11,990.4 $7,451.9 $951.9 $689.3 $1,429.9 $10,523.0 
Balance at June 30, 2021:
Balance at June 30, 2022:Balance at June 30, 2022:
GoodwillGoodwill$9,273.3 $703.2 $814.2 $1,584.7 $12,375.4 Goodwill$7,836.9 $951.9 $689.3 $1,429.9 $10,908.0 
Accumulated impairment lossesAccumulated impairment losses(385.0)(385.0)Accumulated impairment losses(385.0)— — — (385.0)
$8,888.3 $703.2 $814.2 $1,584.7 $11,990.4 $7,451.9 $951.9 $689.3 $1,429.9 $10,523.0 

Intangible assets consist of the following components at June 30, 2021 and December 31, 2020:
(In millions)Weighted Average Life (Years)Original CostAccumulated AmortizationNet Book Value
June 30, 2021
Product rights, licenses and other (1)
15$39,761.5 $11,977.6 $27,783.9 
In-process research and development79.8 — 79.8 
$39,841.3 $11,977.6 $27,863.7 
December 31, 2020
Product rights, licenses and other (1)
15$40,404.1 $10,801.6 $29,602.5 
In-process research and development80.7 — 80.7 
$40,484.8 $10,801.6 $29,683.2 
_______________________
(1)Represents amortizable intangible assets. Other intangible assets consists principally of customer lists and contractual rights.Primarily reflects goodwill relating to the biosimilars portfolio.

The Company hasreviews goodwill for impairment annually on April 1st or more frequently if events or changes in circumstances indicate that the carrying value of goodwill may not be recoverable. As a result of the Biocon Biologics Transaction (refer to Note 6 Balance Sheet Components for additional information) and the decline in the Company’s share price during the first quarter of 2022, the Company performed itsan interim goodwill impairment test as of March 31, 2022. The Company performed the annual goodwill impairment test as of April 1, 20212022. There were no significant changes from the interim goodwill test performed at March 31, 2022 and the results were consistent with the interim goodwill impairment test.
The Company performed both its interim and annual goodwill impairment tests on a quantitative basis for its five reporting units, North America, Europe, Emerging Markets, JANZ, and Greater China. See Note 14, Segment Information, for further discussion. Additionally, the net assets acquired as part of the Combination were included in the respective reporting units and in the annual impairment test for the first time. In estimating each reporting unit’s fair value, the Company performed an extensive valuation analysis, utilizing both income and market-based approaches. The determination of the fair value of the reporting units requires the Company to make significant estimates and assumptions that affect the reporting unit’s expected future cash flows. These estimates and assumptions, utilizing Level 3 inputs, primarily include, but are not limited to, market multiples, control premiums, the discount rate, terminal growth rates, operating income before depreciation and amortization, and capital expenditures forecasts.
As of March 31, 2022 and April 1, 2021,2022, the allocation of the Company’s total goodwill (prior to the reclassification of goodwill to assets held for sale) was as follows: North America $3.66$3.61 billion, Europe $5.15$4.95 billion, Emerging Markets $1.58$1.64 billion, JANZ $0.82$0.78 billion and Greater China $0.70$0.97 billion.


As of March 31, 2022 and April 1, 2022, the Company determined that the fair value of the North America and Greater China reporting units was substantially in excess of the respective unit’s carrying value.
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
As of April 1, 2021, the Company determined that the fair value of the North America, Emerging Markets and Greater China reporting units was substantially in excess of the respective unit’s carrying value.
For the Europe reporting unit, the estimated fair value exceeded its carrying value by approximately $0.91 billion$797 million or 5.8%5.3% for both the interim and annual goodwill impairment test.tests. As it relates to the income approach for the Europe reporting unit at March 31, 2022 and April 1, 2021,2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately 3.0%0.5%. A terminal year value was calculated with a 0.9%negative 1.0% revenue growth rate applied. The discount rate utilized was 10.5%9.5% and the estimated tax rate was 19.0%15.3%. Under the market-based approach, we utilized an estimated range of market multiples of 7.5 to 8.58.0 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by 2.9%3.0% or an increase in discount rate by 1.5% would result in an impairment charge for the Europe reporting unit.

For the JANZ reporting unit, the estimated fair value exceeded its carrying value by approximately $0.23 billion$231 million or 7.0%7.4% for both the interim and annual goodwill impairment test.tests. As it relates to the income approach for the JANZ reporting unit at March 31, 2022 and April 1, 2021,2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately negative 1.5%4.8%. A terminal year value was calculated with a 0.7%assuming no revenue growth rate applied.growth. The discount rate utilized was 8.5%6.0% and the estimated tax rate was 30.5%30.4%. Under the market-based approach, we utilized an estimated market multiple of 6.0 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by 4.2%3.5% or an increase in discount rate by 2.0% would result in an impairment charge for the JANZ reporting unit.
For the Emerging Markets reporting unit, the estimated fair value exceeded its carrying value by approximately $816 million or 10.3% for both the interim and annual goodwill impairment tests. As it relates to the income approach for the Emerging Markets reporting unit at March 31, 2022 and April 1, 2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately 1.6%. A terminal year value was calculated with a 0.8% revenue growth rate applied. The discount rate utilized was 10.5% and the estimated tax rate was 18.4%. Under the market-based approach, we utilized an estimated market multiple of 7.5 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by approximately 8.5% or an increase in discount rate by 3.0% would result in an impairment charge for the Emerging Markets reporting unit.
Due to the inherent uncertainty involved in making these estimates, actual results could differ from those estimates. In addition, changes in underlying assumptions, especially as they relate to the key assumptions detailed, could have a significant impact on the fair value of the reporting units.
Subsequent to the completion of the interim goodwill impairment test, the Company allocated goodwill of $926.9 million as of June 30, 2022 to its biosimilars portfolio using a relative fair value approach and then reclassified the amount to assets held for sale in conjunction with the Biocon Biologics Transaction.
Intangible Assets, Net
Intangible assets consist of the following components at June 30, 2022 and December 31, 2021:
(In millions)Weighted Average Life (Years)Original CostAccumulated AmortizationNet Book Value
June 30, 2022
Product rights, licenses and other (1)
15$37,498.2 $13,440.9 $24,057.3 
In-process research and development43.8 — 43.8 
$37,542.0 $13,440.9 $24,101.1 
December 31, 2021
Product rights, licenses and other (1)
15$39,006.2 $12,918.5 $26,087.7 
In-process research and development46.5 — 46.5 
$39,052.7 $12,918.5 $26,134.2 
____________
(1)Represents amortizable intangible assets. Other intangible assets consists principally of customer lists and contractual rights.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Amortization expense, which is classified primarily within cost of sales in the condensed consolidated statements of operations for the three and six months ended June 30, 20212022 and 20202021 totaled:
Three Months EndedSix Months EndedThree Months EndedSix Months Ended
June 30,June 30,June 30,June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
Intangible asset amortization expenseIntangible asset amortization expense$681.6 $351.6 $1,366.0 $702.8 Intangible asset amortization expense$634.1 $681.6 $1,282.2 $1,366.0 
Intangible asset impairment chargesIntangible asset impairment charges83.4 Intangible asset impairment charges— — — 83.4 
Total intangible asset amortization expense (including impairment charges)Total intangible asset amortization expense (including impairment charges)$681.6 $351.6 $1,449.4 $702.8 Total intangible asset amortization expense (including impairment charges)$634.1 $681.6 $1,282.2 $1,449.4 
On April 30, 2021, the Company completed an agreement to divest a group of OTC products in the U.S. As a result of this transaction, the Company recognized an intangible asset impairment charge of approximately $83.4 million during the six months ended June 30, 2021.
Intangible asset amortization expense over the remainder of 20212022 and for the years endedending December 31, 20222023 through 20252026 is estimated to be as follows:
(In millions)
2021$1,339 
20222,616 
20232,454 
20242,350 
20252,257 
24
(In millions)
2022$1,250 
20232,341 
20242,247 
20252,151 
20262,098 

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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
11.10. 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 certain foreign currency risks, 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 onin 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.
The Company has also entered into forward contracts to hedge forecasted foreign currency denominated sales from certain international subsidiaries and a portion of forecasted intercompany inventory sales denominated in Euro, Japanese Yen and Chinese Renminbi for up to eighteen months. 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 onin the condensed consolidated balance sheets. Any changes in the fair value of designated cash flow hedges are deferred in AOCE and are reclassified into earnings when the hedged item impacts earnings.
Net Investment Hedges
The Company may hedge the foreign currency risk associated with certain net investment positions in foreign subsidiaries by either borrowing directly in foreign currencies and designating all or a portion of the foreign currency debt as a hedge of the applicable net investment position or entering into foreign currency swaps that are designated as hedges of net investments.
The Company has designated certain Euro and Yen borrowings as a hedge of its investment in certain Euro-functional and Yen-functional currency subsidiaries in order to manage foreign currency translation risk. 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. In addition, the Company manages the related foreign exchange risk of the Euro borrowings not designated as net investment hedges through certain Euro denominated financial assets and forward currency swaps.
The following table summarizes the principal amounts of the Company’s outstanding Euro borrowings and the notional amounts of the Euro borrowings designated as net investment hedges:
Notional Amount Designated as a Net Investment Hedge
(In millions)Principal AmountJune 30,
2021
December 31,
2020
2.250% Euro Senior Notes due 20241,000.0 1,000.0 1,000.0 
3.125% Euro Senior Notes due 2028750.0 750.0 750.0 
2.125% Euro Senior Notes due 2025500.0 500.0 500.0 
0.816% Euro Senior Notes due 2022750.0 750.0 750.0 
1.023% Euro Senior Notes due 2024750.0 750.0 750.0 
1.362% Euro Senior Notes due 2027850.0 850.0 850.0 
1.908% Euro Senior Notes due 20321,250.0 1,250.0 1,250.0 
Foreign currency forward contracts105.6 105.6 
Total5,955.6 5,850.0 5,955.6 
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
investments. In addition, the Company manages the related foreign exchange risk of the Euro and Yen borrowings not designated as net investment hedges through certain Euro and Yen denominated financial assets and forward currency swaps.
The following table summarizes the principal amounts of the Company’s outstanding Euro and Yen borrowings and the notional amounts of the Euro and Yen borrowings designated as net investment hedges:
Notional Amount Designated as a Net Investment Hedge
(In millions)Principal AmountJune 30,
2022
December 31,
2021
2.250% Euro Senior Notes due 20241,000.0 1,000.0 1,000.0 
3.125% Euro Senior Notes due 2028750.0 750.0 750.0 
2.125% Euro Senior Notes due 2025500.0 500.0 500.0 
0.816% Euro Senior Notes due 2022 (1)
750.0 — 750.0 
1.023% Euro Senior Notes due 2024750.0 750.0 750.0 
1.362% Euro Senior Notes due 2027850.0 850.0 850.0 
1.908% Euro Senior Notes due 20321,250.0 1,250.0 1,250.0 
Total5,850.0 5,100.0 5,850.0 
Yen
YEN Term Loan¥40,000.0 ¥40,000.0 ¥40,000.0 
Yen Total¥40,000.0 ¥40,000.0 ¥40,000.0 
____________
(1)The Senior Notes were repaid at maturity during the second quarter of 2022.
At June 30, 2022, the principal amount of the Company’s outstanding Yen borrowings and the notional amount of the Yen borrowings designated as net investment hedge was $294.7 million.
Interest Rate Risk Management
The Company enters into interest rate swaps from time to time in order to manage interest rate risk associated with the Company’s fixed-rate and floating-rate debt. Interest rate swaps that meet specific accounting criteria are accounted for as fair value or cash flow hedges. All derivative instruments used to manage interest rate risk are measured at fair value and reported as current assets or current liabilities in the condensed consolidated balance sheets. For fair value hedges, the changes in the fair value of both the hedging instrument and the underlying debt obligations are included in interest expense. For cash flow hedges, the change in fair value of the hedging instrument is deferred through AOCE and is reclassified into earnings when the hedged item impacts earnings.
Credit Risk Management
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 following table summarizes the classification and fair values of derivative instruments in our condensed consolidated balance sheets:
Asset DerivativesLiability Derivatives
(In millions)Balance Sheet LocationJune 30, 2021 Fair ValueDecember 31, 2020 Fair ValueBalance Sheet LocationJune 30, 2021 Fair ValueDecember 31, 2020 Fair Value
Derivatives designated as hedges:
Foreign currency forward contractsPrepaid expenses & other current assets$42.9 $28.3 Other current liabilities$$0.8 
Total derivatives designated as hedges42.9 28.3 0.8 
Derivatives not designated as hedges:
Foreign currency forward contractsPrepaid expenses & other current assets47.4 90.3Other current liabilities40.1 102.8
Total derivatives not designated as hedges47.4 90.340.1 102.8
Total derivatives$90.3 $118.6 $40.1 $103.6 










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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
The following table summarizes the classification and fair values of derivative instruments in our condensed consolidated balance sheets:
Asset DerivativesLiability Derivatives
(In millions)Balance Sheet LocationJune 30, 2022 Fair ValueDecember 31, 2021 Fair ValueBalance Sheet LocationJune 30, 2022 Fair ValueDecember 31, 2021 Fair Value
Derivatives designated as hedges:
Foreign currency forward contractsPrepaid expenses & other current assets$70.6 $62.0 Other current liabilities$2.1 $4.3 
Total derivatives designated as hedges70.6 62.0 2.1 4.3 
Derivatives not designated as hedges:
Foreign currency forward contractsPrepaid expenses & other current assets130.5 82.6Other current liabilities99.8 56.7
Total derivatives not designated as hedges130.5 82.699.8 56.7
Total derivatives$201.1 $144.6 $101.9 $61.0 
The following table summarizes information about the gains/(losses) incurred to hedge or offset operational foreign exchange or interest rate risk:
Amount of Gains/(Losses) Recognized in EarningsAmount of Gains/(Losses) Recognized in AOCE (Net of Tax) on DerivativesAmount of Gains/(Losses) Reclassified from AOCE into Earnings
Three months ended June 30,Three months ended June 30,Three months ended June 30,
(In millions)Location of Gain/(Loss)202120202021202020212020
Derivative Financial Instruments in Cash Flow Hedging Relationships (2) :
Foreign currency forward contracts
Net sales (4)
$— $— $11.3 $12.8 $3.6 $(2.9)
Interest rate swaps
Interest expense (4)
— — (0.9)(1.0)(1.1)
Derivative Financial Instruments in Net Investment Hedging Relationships:
Foreign currency borrowings and forward contracts— — (59.6)(44.9)— — 
Derivative Financial Instruments Not Designated as Hedging Instruments:
Foreign currency option and forward contracts
Other expense, net (3)
(14.9)(16.3)— — — — 
Total$(14.9)$(16.3)$(49.2)$(32.1)$2.6 $(4.0)



Amount of Gains/(Losses) Recognized in EarningsAmount of Gains/(Losses) Recognized in AOCE (Net of Tax) on DerivativesAmount of Gains/(Losses) Reclassified from AOCE into Earnings
Three months ended June 30,Three months ended June 30,Three months ended June 30,
(In millions)Location of Gain/(Loss)202220212022202120222021
Derivative Financial Instruments in Cash Flow Hedging Relationships (1) :
Foreign currency forward contracts
Net sales (3)
$— $— $33.1 $11.3 $28.1 $3.6 
Interest rate swaps
Interest expense (3)
— — (0.8)(0.9)(1.1)(1.0)
Derivative Financial Instruments in Net Investment Hedging Relationships:
Foreign currency borrowings and forward contracts— — 298.6 (59.6)— — 
Derivative Financial Instruments Not Designated as Hedging Instruments:
Foreign currency option and forward contracts
Other expense, net (2)
53.1 (14.9)— — — — 
Total$53.1 $(14.9)$330.9 $(49.2)$27.0 $2.6 
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Amount of Gains/(Losses) Recognized in EarningsAmount of Gains/(Losses) Recognized in AOCE (Net of Tax) on DerivativesAmount of Gains/(Losses) Reclassified from AOCE into EarningsAmount of Gains/(Losses) Recognized in EarningsAmount of Gains/(Losses) Recognized in AOCE (Net of Tax) on DerivativesAmount of Gains/(Losses) Reclassified from AOCE into Earnings
Six months ended June 30,Six months ended June 30,
(In millions)(In millions)Location of Gain/(Loss)202120202021202020212020(In millions)Location of Gain/(Loss)202220212022202120222021
Derivative Financial Instruments in Fair Value Hedge Relationships (1) :
Interest rate swaps
Interest expense (3)
$$22.1 $— $— $— $— 
2023 Senior Notes (3.125% coupon)
Interest expense (3)
(22.1)— — — — 
Derivative Financial Instruments in Cash Flow Hedging Relationships (2) :
Derivative Financial Instruments in Cash Flow Hedging Relationships (1) :
Derivative Financial Instruments in Cash Flow Hedging Relationships (1) :
Foreign currency forward contractsForeign currency forward contracts
Net sales (4)
— — 16.9 (30.0)9.7 (2.8)Foreign currency forward contracts
Net sales (3)
$— $— $42.8 $16.9 $42.3 $9.7 
Interest rate swapsInterest rate swaps
Interest expense (4)
— — (1.7)(2.1)(2.2)Interest rate swaps
Interest expense (3)
— — (1.7)(1.7)(2.2)(2.1)
Derivative Financial Instruments in Net Investment Hedging Relationships:Derivative Financial Instruments in Net Investment Hedging Relationships:Derivative Financial Instruments in Net Investment Hedging Relationships:
Foreign currency borrowings and forward contractsForeign currency borrowings and forward contracts— — 199.0 (4.8)— — Foreign currency borrowings and forward contracts— — 454.9 199.0 — — 
Derivative Financial Instruments Not Designated as Hedging Instruments:Derivative Financial Instruments Not Designated as Hedging Instruments:Derivative Financial Instruments Not Designated as Hedging Instruments:
Foreign currency option and forward contractsForeign currency option and forward contracts
Other expense, net (3)
20.7 13.1 — — — — Foreign currency option and forward contracts
Other expense, net (2)
74.8 20.7 — — — — 
TotalTotal$20.7 $13.1 $214.2 $(34.8)$7.6 $(5.0)Total$74.8 $20.7 $496.0 $214.2 $40.1 $7.6 
____________
(1)In the first quarter of 2020, the Company terminated interest rate swaps designated as a fair value hedge resulting in net proceeds of approximately $45 million. The amount included in the above tables represents the fair value adjustment recognized at the date the interest rate swaps were settled.
(2)At June 30, 2021,2022, the Company expects that approximately $5.0$37.0 million of pre-tax net gains on cash flow hedges will be reclassified from AOCE into earnings during the next twelve months.
(3)(2)Represents the location of the gain/(loss) recognized in earnings on derivatives.
(4)(3)Represents the location of the gain/(loss) reclassified from AOCE into earnings.

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
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 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:
June 30, 2021December 31, 2020 June 30, 2022December 31, 2021
(In millions)(In millions)Level 1Level 2Level 3Level 1Level 2Level 3(In millions)Level 1Level 2Level 3Level 1Level 2Level 3
Recurring fair value measurementsRecurring fair value measurementsRecurring fair value measurements
Financial AssetsFinancial AssetsFinancial Assets
Cash equivalents:Cash equivalents:Cash equivalents:
Money market fundsMoney market funds$0.8 $— $— $0.9 $— $— Money market funds$9.4 $— $— $50.9 $— $— 
Total cash equivalentsTotal cash equivalents0.8 — — 0.9 — — Total cash equivalents9.4 — — 50.9 — — 
Equity securities:Equity securities:Equity securities:
Exchange traded fundsExchange traded funds48.9 — — 45.1 — — Exchange traded funds41.5 — — 50.3 — — 
Marketable securitiesMarketable securities0.7 — — 0.7 — — Marketable securities0.2 — — 0.7 — — 
Total equity securitiesTotal equity securities49.6 — — 45.8 — — Total equity securities41.7 — — 51.0 — — 
Available-for-sale fixed income investments:Available-for-sale fixed income investments:Available-for-sale fixed income investments:
Corporate bondsCorporate bonds— 17.6 — — 17.8 — Corporate bonds— 16.2 — — 16.6 — 
U.S. TreasuriesU.S. Treasuries— 13.5 — — 14.4 — U.S. Treasuries— 11.9 — — 14.6 — 
Agency mortgage-backed securitiesAgency mortgage-backed securities— 1.6 — — 1.9 — Agency mortgage-backed securities— 3.2 — — 2.0 — 
Asset backed securitiesAsset backed securities— 5.3 — — 4.6 — Asset backed securities— 3.7 — — 4.6 — 
OtherOther— 0.5 — — 0.4 — Other— 0.5 — — 0.4 — 
Total available-for-sale fixed income investmentsTotal available-for-sale fixed income investments— 38.5 — — 39.1 — Total available-for-sale fixed income investments— 35.5 — — 38.2 — 
Foreign exchange derivative assetsForeign exchange derivative assets— 90.3 — — 118.6 — Foreign exchange derivative assets— 201.1 — — 144.6 — 
Total assets at recurring fair value measurementTotal assets at recurring fair value measurement$50.4 $128.8 $— $46.7 $157.7 $— Total assets at recurring fair value measurement$51.1 $236.6 $— $101.9 $182.8 $— 
Financial LiabilitiesFinancial LiabilitiesFinancial Liabilities
Foreign exchange derivative liabilitiesForeign exchange derivative liabilities— 40.1 — — 103.6 — Foreign exchange derivative liabilities— 101.9 — — 61.0 — 
Contingent considerationContingent consideration— — 213.8 — — 223.6 Contingent consideration— — 181.0 — — 199.7 
Total liabilities at recurring fair value measurementTotal liabilities at recurring fair value measurement$— $40.1 $213.8 $— $103.6 $223.6 Total liabilities at recurring fair value measurement$— $101.9 $181.0 $— $61.0 $199.7 

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
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.
Equity securities, exchange traded funds — valued at the active quoted market prices from broker or dealer quotations or transparent pricing sources at the reporting date. Unrealized gains and losses attributable to changes in fair value are included in other expense, net, in the condensed consolidated statements of operations.
Equity securities, marketable securities — valued using quoted stock prices from public exchanges at the reporting date. Unrealized gains and losses attributable to changes in fair value are included in other expense, net, in the condensed consolidated statements of operations.
Available-for-sale fixed income investments — valued at the quoted market prices from broker or dealer quotations or transparent pricing sources at the reporting date. Unrealized gains and losses attributable to changes in fair value, net of income taxes, are included in accumulated other comprehensive loss as a component of shareholders’ equity.
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 Pfizer’s respiratory delivery platform and certain other acquisitions. The measurement is calculated using unobservable inputs based on the Company’s own assumptions primarily related to the probability and timing of future development and commercial milestones and future profit sharing payments which are discounted using a market rate of return. At June 30, 20212022 and December 31, 2020,2021, discount rates ranging from 2.1%8.0% to 10.5%8.5% were utilized in the valuations. Significant changes in unobservable inputs could result in material changes to the contingent consideration liability.
A rollforward of the activity in the Company’s fair value of contingent consideration from December 31, 20202021 to June 30, 20212022 is as follows:
(In millions)(In millions)
Current Portion (1)
Long-Term Portion (2)
Total Contingent Consideration(In millions)
Current Portion (1)
Long-Term Portion (2)
Total Contingent Consideration
Balance at December 31, 2020$100.5 $123.1 $223.6 
Balance at December 31, 2021Balance at December 31, 2021$66.7 $133.0 $199.7 
PaymentsPayments(46.6)(46.6)Payments(36.0)— (36.0)
ReclassificationsReclassifications29.2 (29.2)Reclassifications43.1 (43.1)— 
AccretionAccretion4.8 4.8 Accretion— 3.7 3.7 
Fair value loss (3)
Fair value loss (3)
32.0 32.0 
Fair value loss (3)
— 13.6 13.6 
Balance at June 30, 2021$83.1 $130.7 $213.8 
Balance at June 30, 2022Balance at June 30, 2022$73.8 $107.2 $181.0 
____________
(1)Included in other current liabilities in the condensed consolidated balance sheets.
(2)Included in other long-term obligations in the condensed consolidated balance sheets.
(3)Included in litigation settlements and other contingencies, net in the condensed consolidated statements of operations.
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.

11.
Debt

For additional information, see Note 10
Debt in Viatris’ 2021 Form 10-K.

Short-Term Borrowings
The Company had $1.02 billion and $1.49 billion of short-term borrowings as of June 30, 2022 and December 31, 2021, respectively.
(In millions)June 30,
2022
December 31,
2021
Commercial paper notes$620.8 $1,173.4 
Receivables Facility198.7 318.5 
Note Securitization Facility200.0 — 
Other0.2 1.1 
Short-term borrowings$1,019.7 $1,493.0 
Receivables Facility
The Company has a $400 million Receivables Facility (the “Receivables Facility”), which originally was to expire on April 22, 2022. On April 22, 2022, the Company entered into an agreement to extend the expiration date of the Receivables Facility to April 22, 2025.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
12.DebtUnder the terms of the Receivables Facility, our subsidiary, MPI, sells certain accounts receivable to Mylan Securitization LLC (“Mylan Securitization”), a wholly-owned special purpose entity which in turn sells a percentage ownership interest in the receivables to financial institutions and commercial paper conduits sponsored by financial institutions. Mylan Securitization’s assets have been pledged to MUFG Bank, Ltd., as agent, in support of its obligations under the Receivables Facility. Any amounts outstanding under the facility are recorded as borrowings and the underlying receivables are included in accounts receivable, net, in the condensed consolidated balance sheets.
Short-Term Borrowings
The Company had $1.30 billion and $1.10 billion of short-term borrowings as of June 30, 2021 and December 31, 2020, respectively.
(In millions)June 30,
2021
December 31,
2020
Commercial paper notes$700.5 $651.3 
Receivables Facility400.0 248.4 
Note Securitization Facility200.0 200.0 
Other1.2 
Short-term borrowings$1,300.5 $1,100.9 
Long-Term Debt
For additional information, see Note 10 A summary of long-term debt is as follows:Debt in Viatris’ 2020 Form 10-K.
($ in millions)Interest Rate as of June 30, 2022June 30,
2022
December 31,
2021
Current portion of long-term debt:
2022 Euro Senior Notes (a) ****
0.816 %$— $856.6 
2022 Senior Notes (b) ***
1.125 %— 1,002.9 
2023 Senior Notes (c) *
3.125 %758.3 — 
Other0.8 0.9 
Deferred financing fees(0.5)(0.1)
Current portion of long-term debt$758.6 $1,860.3 
Non-current portion of long-term debt:
2023 Senior Notes (c) *
3.125 %— 766.1 
2023 Senior Notes *
4.200 %499.7 499.6 
2024 Euro Senior Notes **
2.250 %1,047.5 1,135.8 
2024 Euro Senior Notes ****
1.023 %800.2 871.6 
2025 Euro Senior Notes *
2.125 %523.7 567.8 
2025 Senior Notes ***
1.650 %761.5 763.4 
2026 Senior Notes **
3.950 %2,242.3 2,241.4 
2027 Euro Senior Notes ****
1.362 %930.2 1,013.0 
2027 Senior Notes ***
2.300 %778.1 780.8 
2028 Euro Senior Notes **
3.125 %781.7 847.4 
2028 Senior Notes *
4.550 %748.8 748.7 
2030 Senior Notes ***
2.700 %1,516.7 1,520.5 
2032 Euro Senior Notes ****
1.908 %1,421.3 1,546.6 
2040 Senior Notes ***
3.850 %1,653.8 1,657.1 
2043 Senior Notes *
5.400 %497.4 497.3 
2046 Senior Notes **
5.250 %999.9 999.9 
2048 Senior Notes *
5.200 %747.8 747.8 
2050 Senior Notes ***
4.000 %2,202.9 2,205.1 
YEN Term Loan Facility294.7 347.6 
Revolving Facility795.0 — 
Other1.7 1.9 
Deferred financing fees(38.5)(42.3)
Long-term debt$19,206.4 $19,717.1 
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Long-Term Debt
A summary of long-term debt is as follows:
($ in millions)Interest Rate as of June 30, 2021June 30,
2021
December 31,
2020
Current portion of long-term debt:
2021 Senior Notes (a) **
3.150 %2,249.7 
2022 Euro Senior Notes ****
0.816 %897.5 
2022 Senior Notes ***
1.125 %1,005.9 
USD Term Loan240.0 
Other5.0 8.0 
Deferred financing fees(1.4)
Current portion of long-term debt$2,148.4 $2,256.3 
Non-current portion of long-term debt:
2022 Euro Senior Notes ****
0.816 %928.8 
2022 Senior Notes ***
1.125 %1,008.8 
2023 Senior Notes (b) *
3.125 %773.8 781.6 
2023 Senior Notes *
4.200 %499.5 499.3 
2024 Euro Senior Notes **
2.250 %1,184.4 1,219.9 
2024 Euro Senior Notes ****
1.023 %913.0 944.6 
2025 Euro Senior Notes *
2.125 %592.1 609.9 
2025 Senior Notes ***
1.650 %765.2 767.1 
2026 Senior Notes **
3.950 %2,240.6 2,239.7 
2027 Euro Senior Notes ****
1.362 %1,060.9 1,097.4 
2027 Senior Notes ***
2.300 %783.5 786.1 
2028 Euro Senior Notes **
3.125 %883.4 909.7 
2028 Senior Notes *
4.550 %748.7 748.6 
2030 Senior Notes ***
2.700 %1,524.3 1,528.0 
2032 Euro Senior Notes ****
1.908 %1,618.3 1,672.6 
2040 Senior Notes ***
3.850 %1,660.3 1,663.3 
2043 Senior Notes *
5.400 %497.3 497.3 
2046 Senior Notes **
5.250 %999.9 999.9 
2048 Senior Notes *
5.200 %747.7 747.7 
2050 Senior Notes ***
4.000 %2,207.2 2,209.3 
USD Term Loan360.0 600.0 
2020 Revolving Facility900.0 
Other1.6 17.4 
Deferred financing fees(44.7)(47.8)
Long-term debt$20,917.0 $22,429.2 
____________
(a)    The 20212022 Euro Senior Notes were repaid at maturity in the second quarter of 2021.2022.
(b)The 2022 Senior Notes were repaid at maturity in the second quarter of 2022.
(c)    In the first quarter of 2020, the Company terminated interest rate swaps designated as a fair value hedge resulting in net proceeds of approximately $45 million. The fair value adjustment is being amortized to interest expense over the remaining term of the notes.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
*    Instrument was issued by Mylan Inc.
**    Instrument was originally issued by Mylan N.V.; now held by Utah Acquisition Sub Inc.
***     Instrument was issued by Viatris Inc.
****     Instrument was issued by Upjohn Finance B.V.
For additional information, see Note 10
Debt in Viatris’ 2020 Form 10-K.
USD Term Loan, 2020 Revolving Facility, YEN Term Loan and 2021 Revolving Facility
In June 2020, Viatris entered into (i) a $600 million term loan agreement (the “USD Term Loan”) and (ii) a $4.0 billion revolving facility (the “2020 Revolving Facility”) with various syndicates of banks. The USD Term Loan was fully repaid in July 2021.
The USD Term Loan and the 2020 Revolving Facility contained a maximum consolidated leverage ratio financial covenant requiring maintenance of a maximum ratio of consolidated total indebtedness as of the end of any quarter to consolidated EBITDA for the trailing four quarters as defined in the related credit agreements. The maximum leverage ratio is 4.25 to 1.00 for the first four full fiscal quarters following the close of the Combination and 3.75 to 1.00 thereafter, except in circumstances as defined in the related credit agreements.
The USD Term Loan and the 2020 Revolving Facility contained 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.
In July 2021, Viatris entered into (i) a ¥40 billion term loan credit agreement (the “YEN Term Loan”) and (ii) a $4.0 billion revolving credit agreement (the “2021 Revolving Facility”) with various syndicates of banks. The 2021 Revolving Facility amended and restated the 2020 Revolving Facility and proceeds from the 2021 Revolving Facility were used to repay outstanding obligations under the 2020 Revolving Facility. Proceeds from the YEN Term Loan and 2021 Revolving Facility were also used to repay the USD Term Loan in full and the USD Term Loan was terminated. The 2021 Revolving Facility and the YEN Term Loan have substantially identical terms to the 2020 Revolving Facility and USD Term Loan, respectively with the following exceptions: 1) the maturity of both the YEN Term Loan and the 2021 Revolving Facility is July 2026, 2) the pricing was adjusted to reflect current market prices (which were generally more favorable) and 3) the maximum leverage ratio as of the end of any quarter was set at 4.25 to 1.00 for each quarter ending after June 30, 2021 through and including June 30, 2022, 4.0 to 1.00 for each quarter ending after June 30, 2022 through and including December 31, 2022 and 3.75 to 1.00 thereafter, except in circumstances as defined in the related credit agreement. The Company expects to designate the YEN Term Loan as a hedge of its investment in certain Yen-functional currency subsidiaries in order to manage foreign currency translation risk.
The YEN Term Loan and the 2021 Revolving Facility contain customary affirmative covenants for facilities of this type, including among others, those set forth above with respect to the USD Term Loan and the 2020 Revolving Facility.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Fair Value
At June 30, 20212022 and December 31, 2020,2021, the aggregate fair value of the Company’s outstanding notes was approximately $22.53$15.58 billion and $25.90$22.01 billion, respectively. The fair values of the outstanding notes were valued at quoted market prices from broker or dealer quotations and were classified as Level 2 in the fair value hierarchy.
Mandatory minimum repayments remaining on the notional amount of outstanding long-term debt at June 30, 20212022 were as follows for each of the periods ending December 31:
(In millions)(In millions)Total(In millions)Total
2021$
202220222,489 2022$— 
202320232,150 20231,250 
202420242,075 20241,835 
202520251,343 20251,274 
202620263,340 
ThereafterThereafter14,330 Thereafter11,688 
TotalTotal$22,387 Total$19,387 
13.12.Comprehensive Loss
Accumulated other comprehensive loss, as reflected on the condensed consolidated balance sheets, is comprised of the following:
(In millions)June 30,
2022
December 31,
2021
Accumulated other comprehensive loss:
Net unrealized loss on marketable securities, net of tax$(2.1)$— 
Net unrecognized gain and prior service cost related to defined benefit plans, net of tax30.1 32.2 
Net unrecognized gain on derivatives in cash flow hedging relationships, net of tax22.7 9.2 
Net unrecognized gain on derivatives in net investment hedging relationships, net of tax471.6 16.7 
Foreign currency translation adjustment(3,421.5)(1,802.4)
$(2,899.2)$(1,744.3)

(In millions)June 30,
2021
December 31,
2020
Accumulated other comprehensive loss:
Net unrealized gain on marketable securities, net of tax$0.4 $1.2 
Net unrecognized gain (loss) and prior service cost related to defined benefit plans, net of tax43.6 (26.1)
Net unrecognized loss on derivatives in cash flow hedging relationships, net of tax(6.2)(18.0)
Net unrecognized loss on derivatives in net investment hedging relationships, net of tax(220.8)(353.6)
Foreign currency translation adjustment(1,022.0)(461.5)
$(1,205.0)$(858.0)








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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Components of accumulated other comprehensive loss, before tax, consist of the following, for the three and six months ended June 30, 20212022 and 2020:2021:

Three Months Ended June 30, 2022
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at March 31, 2022, net of tax$9.4 $173.1 $(1.3)$29.4 $(2,271.6)$(2,061.0)
Other comprehensive earnings (loss) before reclassifications, before tax44.6 384.4 (1.0)0.4 (1,149.9)(721.5)
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(28.1)(28.1)(28.1)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense1.1 1.1 1.1 
Amortization of actuarial loss included in SG&A0.1 0.1 
Net other comprehensive earnings (loss), before tax17.6 384.4 (1.0)0.5 (1,149.9)(748.4)
Income tax provision (benefit)4.3 85.9 (0.2)(0.2)— 89.8 
Balance at June 30, 2022, net of tax$22.7 $471.6 $(2.1)$30.1 $(3,421.5)$(2,899.2)
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Six Months Ended June 30, 2022
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at December 31, 2021, net of tax$9.2 $16.7 $— $32.2 $(1,802.4)$(1,744.3)
Other comprehensive earnings (loss) before reclassifications, before tax57.9 585.7 (2.7)(2.3)(1,619.1)(980.5)
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(42.3)(42.3)(42.3)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense2.2 2.2 2.2 
Amortization of prior service costs included in SG&A0.1 0.1 
Amortization of actuarial loss included in SG&A0.1 0.1 
Net other comprehensive earnings (loss), before tax17.8 585.7 (2.7)(2.1)(1,619.1)(1,020.4)
Income tax provision (benefit)4.3 130.8 (0.6)— — 134.5 
Balance at June 30, 2022, net of tax$22.7 $471.6 $(2.1)$30.1 $(3,421.5)$(2,899.2)

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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Three Months Ended June 30, 2021
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at March 31, 2021, net of tax$(15.5)$(161.3)$0.2 $(26.3)$(1,182.7)$(1,385.6)
Other comprehensive earnings (loss) before reclassifications, before tax15.0 (77.4)0.2 72.2 160.7 170.7 
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(3.6)(3.6)(3.6)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense1.0 1.0 1.0 
Amortization of prior service costs included in SG&A(0.2)(0.2)
Amortization of actuarial gain included in SG&A0.5 0.5 
Net other comprehensive earnings (loss), before tax12.4 (77.4)0.2 72.5 160.7 168.4 
Income tax provision (benefit)3.1 (17.9)2.6 (12.2)
Balance at June 30, 2021, net of tax$(6.2)$(220.8)$0.4 $43.6 $(1,022.0)$(1,205.0)

Three Months Ended June 30, 2021
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at March 31, 2021, net of tax$(15.5)$(161.3)$0.2 $(26.3)$(1,182.7)$(1,385.6)
Other comprehensive earnings (loss) before reclassifications, before tax15.0 (77.4)0.2 72.2 160.7 170.7 
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(3.6)(3.6)(3.6)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense1.0 1.0 1.0 
Amortization of prior service costs included in SG&A(0.2)(0.2)
Amortization of actuarial loss included in SG&A0.5 0.5 
Net other comprehensive earnings (loss), before tax12.4 (77.4)0.2 72.5 160.7 168.4 
Income tax provision (benefit)3.1 (17.9)— 2.6 — (12.2)
Balance at June 30, 2021, net of tax$(6.2)$(220.8)$0.4 $43.6 $(1,022.0)$(1,205.0)
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VIATRIS INC. AND SUBSIDIARIES
Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Three Months Ended June 30, 2020
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at March 31, 2020, net of tax$(70.1)$(34.1)$0.8 $(19.0)$(2,331.1)$(2,453.5)
Other comprehensive earnings (loss) before reclassifications, before tax14.7 (47.3)0.6 6.5 452.0 426.5 
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales2.9 2.9 2.9 
Loss on interest rate swaps classified as cash flow hedges, included in interest expense1.1 1.1 1.1 
Amortization of actuarial loss included in SG&A0.1 0.1 
Net other comprehensive earnings (loss), before tax18.7 (47.3)0.6 6.6 452.0 430.6 
Income tax provision (benefit)4.3 (2.4)0.1 2.0 
Balance at June 30, 2020, net of tax$(55.7)$(79.0)$1.3 $(12.4)$(1,879.1)$(2,024.9)
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Six Months Ended June 30, 2021
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at December 31, 2020, net of tax$(18.0)$(353.6)$1.2 $(26.1)$(461.5)$(858.0)
Other comprehensive earnings (loss) before reclassifications, before tax23.3 150.0 (0.7)72.8 (560.5)(315.1)
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(9.7)(9.7)(9.7)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense2.1 2.1 2.1 
Amortization of prior service costs included in SG&A(0.3)(0.3)
Amortization of actuarial loss included in SG&A0.8 0.8 
Net other comprehensive earnings (loss), before tax15.7 150.0 (0.7)73.3 (560.5)(322.2)
Income tax provision (benefit)3.9 17.2 0.1 3.6 24.8 
Balance at June 30, 2021, net of tax$(6.2)$(220.8)$0.4 $43.6 $(1,022.0)$(1,205.0)
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
Six Months Ended June 30, 2020
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at December 31, 2019, net of tax$(31.6)$(74.3)$0.6 $(17.4)$(1,674.5)$(1,797.2)
Other comprehensive (loss) earnings before reclassifications, before tax(37.7)(5.0)0.8 4.7 (204.6)(241.8)
Amounts reclassified from accumulated other comprehensive (loss) earnings, before tax:
Loss on foreign exchange forward contracts classified as cash flow hedges, included in net sales2.8 2.8 2.8 
Loss on interest rate swaps classified as cash flow hedges, included in interest expense2.2 2.2 2.2 
Amortization of actuarial loss included in SG&A0.3 0.3 
Net other comprehensive (loss) earnings, before tax(32.7)(5.0)0.8 5.0 (204.6)(236.5)
Income tax (benefit) provision(8.6)(0.3)0.1 (8.8)
Balance at June 30, 2020, net of tax$(55.7)$(79.0)$1.3 $(12.4)$(1,879.1)$(2,024.9)
Six Months Ended June 30, 2021
Gains and Losses on Derivatives in Cash Flow Hedging RelationshipsGains and Losses on Net Investment HedgesGains and Losses on Marketable SecuritiesDefined Pension Plan ItemsForeign Currency Translation AdjustmentTotals
(In millions)Foreign Currency Forward ContractsInterest Rate SwapsTotal
Balance at December 31, 2020, net of tax$(18.0)$(353.6)$1.2 $(26.1)$(461.5)$(858.0)
Other comprehensive earnings (loss) before reclassifications, before tax23.3 150.0 (0.7)72.8 (560.5)(315.1)
Amounts reclassified from accumulated other comprehensive earnings (loss), before tax:
Gain on foreign exchange forward contracts classified as cash flow hedges, included in net sales(9.7)(9.7)(9.7)
Loss on interest rate swaps classified as cash flow hedges, included in interest expense2.1 2.1 2.1 
Amortization of prior service costs included in SG&A(0.3)(0.3)
Amortization of actuarial loss included in SG&A0.8 0.8 
Net other comprehensive earnings (loss), before tax15.7 150.0 (0.7)73.3 (560.5)(322.2)
Income tax provision3.9 17.2 0.1 3.6 — 24.8 
Balance at June 30, 2021, net of tax$(6.2)$(220.8)$0.4 $43.6 $(1,022.0)$(1,205.0)
14.13.Segment Information
Viatris has four reportable segments: Developed Markets, Greater China, JANZ, and Emerging Markets. The Company reports segment information on the basis of markets and geography. In conjunction with the formation of Viatris, the Company has changedgeography, which reflects its reportable segments, from North America, Europe, and Rest of World, to Developed Markets, Greater China, JANZ, and Emerging Markets. Prior year amounts have been recasted to reflect this segment structure. We have also revised our measure of segment profitability. This approach reflects the Company’s focus on bringing its broad and diversified portfolio of branded, complex generics and biosimilars, and generic products to people in markets everywhere. Our Developed Markets segment comprises our operations primarily in North America and Europe. Our Greater China segment includes our operations in China, Taiwan and Hong Kong. Our JANZ segment reflects our operations in Japan, Australia and New Zealand. Our Emerging Markets segment encompasses our operationspresence in more than 125 countries with developing markets and emerging economies including countries in Asia, Africa, Eastern Europe, Latin America and the Middle East South and Central America, Africa and Eastern Europe, and also includesas well as the Company’s anti-retroviralARV franchise.
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.
Certain costs are not included in the measurement of segment profitability, such as costs, if any, associated with the following:
Intangible asset amortization expense and impairments of intangible assets;
R&D expense;
Net charges or net gains for litigation settlements and other contingencies;
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Net charges or net gains for litigation settlements and other contingencies;
Certain costs related to transactions and events such as (i) purchase accounting adjustments, where we incur expenses associated with the amortization of fair value adjustments to inventory and property, plant and equipment; (ii) acquisition-related costs, where we incur costs for executing the transaction, integrating the acquired operations and restructuring the combined company; and (iii) other significant items, which are substantive and/or unusual, and in some cases recurring, items (such as restructuring) that are evaluated on an individual basis by management and that either as a result of their nature or size, would not be expected to occur as part of our normal business on a regular basis. Such special items can include, but are not limited to, non-acquisition-related restructuring costs, as well as costs incurred for asset impairments and disposals of assets or businesses, including, as applicable, any associated transition activities.
Corporate and other unallocated costs associated with platform functions (such as digital, facilities, legal, finance, human resources, insurance, public affairs and procurement), patient advocacy activities and certain compensation and other corporate costs (such as interest income and expense, and gains and losses on investments, as well as overhead expenses associated with our manufacturing, which include manufacturing variances associated with production) and operations that are not directly assessed to an operating segment as business unit (segment) management does not manage these costs.
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 Note 2 Summary of Significant Accounting Policies included in the 20202021 Form 10-K, and Note 3 Recent Accounting Pronouncements, Adoption of New Accounting Standards included in this Form 10-Q.10-K.
Presented in the table below is segment information for the periods identified and a reconciliation of segment information to total consolidated information.
Net SalesSegment Profitability
Three Months Ended June 30,Three Months Ended June 30,
(In millions)2021202020212020
Reportable Segments:
Developed Markets$2,640.4 $1,982.7 $1,319.9 $1,048.6 
Greater China550.3 22.7 366.5 5.5 
JANZ501.0 280.2 185.4 83.4 
Emerging Markets870.0 410.3 384.7 133.4 
Total reportable segments$4,561.7 $2,695.9 $2,256.5 $1,270.9 
Reconciling items:
Intangible asset amortization expense(681.6)(351.6)
Globally managed research and development costs(147.7)(156.3)
Litigation settlements & other contingencies(23.0)(15.8)
Transaction related and other special items(920.7)(269.6)
Corporate and other unallocated(531.3)(343.4)
(Loss) earnings from operations$(47.8)$134.2 


Net SalesSegment Profitability
Three Months Ended June 30,Three Months Ended June 30,
(In millions)2022202120222021
Reportable Segments:
Developed Markets$2,479.1 $2,640.4 $1,255.3 $1,319.9 
Greater China548.3 550.3 392.8 366.5 
JANZ427.1 501.0 158.1 185.4 
Emerging Markets650.9 870.0 301.0 384.7 
Total reportable segments$4,105.4 $4,561.7 $2,107.2 $2,256.5 
Reconciling items:
Intangible asset amortization expense(634.1)(681.6)
Globally managed research and development costs(162.6)(147.7)
Litigation settlements & other contingencies(10.9)(23.0)
Transaction related and other special items(227.1)(920.7)
Corporate and other unallocated(523.8)(531.3)
Earnings (loss) from operations$548.7 $(47.8)
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Net SalesSegment ProfitabilityNet SalesSegment Profitability
Six Months Ended June 30,Six Months Ended June 30,Six Months Ended June 30,Six Months Ended June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
Reportable Segments:Reportable Segments:Reportable Segments:
Developed MarketsDeveloped Markets$5,212.0 $3,969.1 $2,605.3 $2,037.6 Developed Markets$4,955.2 $5,212.0 $2,466.8 $2,605.3 
Greater ChinaGreater China1,142.2 37.8 771.4 5.1 Greater China1,121.4 1,142.2 810.5 771.4 
JANZJANZ982.9 523.4 369.6 135.0 JANZ850.9 982.9 332.4 369.6 
Emerging MarketsEmerging Markets1,624.7 753.8 722.0 228.2 Emerging Markets1,356.1 1,624.7 646.3 722.0 
Total reportable segmentsTotal reportable segments$8,961.8 $5,284.1 $4,468.3 $2,405.9 Total reportable segments$8,283.6 $8,961.8 $4,256.0 $4,468.3 
Reconciling items:Reconciling items:Reconciling items:
Intangible asset amortization expenseIntangible asset amortization expense(1,366.0)(702.8)Intangible asset amortization expense(1,282.2)(1,366.0)
Intangible asset impairment chargesIntangible asset impairment charges(83.4)Intangible asset impairment charges— (83.4)
Globally managed research and development costsGlobally managed research and development costs(331.8)(270.5)Globally managed research and development costs(304.9)(331.8)
Litigation settlements & other contingenciesLitigation settlements & other contingencies(45.9)(17.6)Litigation settlements & other contingencies(17.1)(45.9)
Transaction related and other special itemsTransaction related and other special items(1,914.1)(433.8)Transaction related and other special items(412.7)(1,914.1)
Corporate and other unallocatedCorporate and other unallocated(1,041.1)(662.3)Corporate and other unallocated(983.0)(1,041.1)
(Loss) earnings from operations$(314.0)$318.9 
Earnings (loss) from operationsEarnings (loss) from operations$1,256.1 $(314.0)

15.14.Restructuring
2020 Restructuring Program
During the fourth quarter of 2020, Viatris announced a significant global restructuring program in order to achieve synergies and ensure that the organization is optimally structured and efficiently resourced to deliver sustainable value to patients, shareholders, customers, and other stakeholders. Viatris’ restructuring initiative incorporates and expands onAs part of the restructuring, program announced by Mylan N.V. earlier in 2020 as part of its business transformation efforts. Thethe Company expects to optimizeis optimizing its commercial capabilities and enabling functions, and close, downsizeclosing, downsizing or divest up to 15divesting certain manufacturing facilities globally that are deemed to be no longer viable either due to surplus capacity, challenging market dynamics or a shift in its product portfolio toward more complex products. As a result, Viatris expects that up to 20% of its global workforce may be impacted upon completion of the restructuring initiative.
For the committed restructuring actions, the Company expects to incur total pre-tax charges ranging between $1.1 billion andof up to approximately $1.4 billion. Such charges are expected to include between $350 million andup to approximately $450 million of non-cash charges mainly related to accelerated depreciation and asset impairment charges, including inventory write-offs. The remaining estimated cash costs of between $750 million andup to approximately $950 million are expected to be primarily related to severance and employee benefits expense, as well as other costs, including those related to contract terminations and decommissioningother plant disposal costs.

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 have been met.
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The following table summarizes the restructuring charges and the reserve activity for the 2020 restructuring program from December 31, 20202021 to June 30, 2021:2022:
(In millions)(In millions)Employee Related CostsOther Exit CostsTotal(In millions)Employee Related CostsOther Exit CostsTotal
Balance at December 31, 2020:$262.6 $4.8 $267.4 
Balance at December 31, 2021:Balance at December 31, 2021:$292.6 $4.1 $296.7 
Charges (1)
Charges (1)
161.6 152.0 313.6 
Charges (1)
7.3 9.5 16.8 
Cash paymentCash payment(49.2)(1.1)(50.3)Cash payment(77.6)(6.2)(83.8)
UtilizationUtilization(151.0)(151.0)Utilization— (4.2)(4.2)
Foreign currency translationForeign currency translation(3.3)0.1 (3.2)Foreign currency translation(2.1)(0.1)(2.2)
Balance at March 31, 2021:$371.7 $4.8 $376.5 
Balance at March 31, 2022:Balance at March 31, 2022:$220.2 $3.1 $223.3 
Charges (1)
Charges (1)
169.0 82.9 251.9 
Charges (1)
4.0 5.8 9.8 
Reimbursable restructuring charges26.4 26.4 
Cash paymentCash payment(74.7)(2.1)(76.8)Cash payment(36.9)(2.3)(39.2)
UtilizationUtilization(80.8)(80.8)Utilization— (3.9)(3.9)
Foreign currency translationForeign currency translation1.6 (0.1)1.5 Foreign currency translation(3.6)(0.1)(3.7)
Balance at June 30, 2021:$494.0 $4.7 $498.7 
Balance at June 30, 2022:Balance at June 30, 2022:$183.7 $2.6 $186.3 
____________
(1)     For the three months ended June 30, 2021,2022, total restructuring charges in Developed Markets, JANZ, Emerging Markets, Greater China, JANZ and Corporate/Other were approximately $115.1$7.6 million, $107.5$1.1 million, $6.0$0.8 million, $0.2 million, and $23.3$0.1 million, respectively.
For the six months ended June 30, 2021,2022, total restructuring charges in Developed Markets, Emerging Markets, Greater China, JANZ, Emerging Markets, and Corporate/Other were approximately $381.6$20.3 million, $5.3$3.7 million, $109.0$2.1 million, $46.3$0.3 million, and $23.3$0.2 million, respectively.
At June 30, 20212022 and December 31, 2020,2021, accrued liabilities for restructuring and other cost reduction programs were primarily included in other current liabilities and other long-term obligations in the condensed consolidated balance sheets.

16.15.CollaborationLicensing and LicensingOther Partner Agreements
We periodically enter into collaborationlicensing and licensingother partner agreements with other pharmaceutical companies for the development, manufacture, marketing and/or sale of pharmaceutical products. Our significant collaborationlicensing and licensingother partner agreements are primarily focused on the development, manufacturing, supply and commercialization of multiple, high-value generic biologic compounds, insulin analog products and respiratory products, among other complex 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 obligations reflected as acquisition related contingent consideration. Refer to Note 1110 Financial Instruments and Risk Management for further discussion of contingent consideration.
Our potential maximum development milestones not accrued for at June 30, 20212022 totaled approximately $359$338 million. We estimate that the amounts that may be paid through the end of 20212022 to be approximately $24$10 million. 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 amounts disclosed do not include sales-based milestones or royalty or profit share 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 or profit share obligations may be significant depending upon the level of commercial sales for each product.
There have been no significant changes to our collaborationlicensing and licensingother partner agreements as disclosed in Note 18 of our 20202021 Form 10-K.
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17.16.Income Taxes
Tax Examinations
The Company is subject to income taxes and tax audits in many jurisdictions. A certain degree of estimation is thus required in recording the assets and liabilities related to income taxes. Tax audits and examinations can involve complex issues, interpretations, and judgments and the resolution of matters that may span multiple years, particularly if subject to litigation or negotiation.
Although the Company believes that adequate provisions have been made for these uncertain tax positions, the Company’s assessment of uncertain tax positions, including those arising from legal entity restructuring transactions in connection with the Combination, is based on estimates and assumptions that the Company believes are reasonable but the estimates for unrecognized tax benefits and potential tax benefits may not be representative of actual outcomes, and variations from such estimates could materially affect the Company’s financial condition, results of operations or cash flows in the period of resolution, settlement or when the statutes of limitations expire.
The Company is subject to ongoing IRS examinations. The years 2015 through 20182019 are open years under examination. The years 2012, 2013 and 2014 have one matter open, and a Tax Court petition was filed regarding the matter and a trial was held in December 2018 and is discussed further below.
Several international audits are currently in progress. In some cases, the tax auditors have proposed adjustments or issued assessments to our tax positions, including with respect to intercompany transactions, and we are in ongoing discussions with some of the auditors regarding the validity of their positions.
In instances where assessments have been issued, we disagree with these assessments and believe they are without merit and incorrect as a matter of law. As a result, we anticipate that certain of these matters may become the subject of litigation before tax courts where we intend to vigorously defend our position.
In Australia, the tax authorities have issued notices of assessments to the Company for the years ended December 2009 to December 2019,2020, subject to additional interest and penalties, concerning our tax position with respect to certain intercompany transactions. The tax authorities denied our objections to the assessments for the years ended December 2009 to December 2019 and we have commenced litigation in the Australian Federal Court challenging that decision. On July 28, 2022, we received notice that the tax authority has denied our objection for the year ended December 2020. We intend to challenge these assessments in courtinclude the year ended December 2020 in the event our objections are not sustained.litigation which has already commenced for years ended December 2009 to December 2019. The Company made a partial payment of $56.0 million in 2021 and $5.2 million in 2022 in order to stay potential interest and penalties resulting from this litigation.

In France, the tax authorities have issued notices of assessments to the Company for the years ended December 2013 to December 20162015 concerning our tax position with respect to (i) certain intercompany transactions and (ii) whether income earned by a Company entity not domiciled in France should be subject to French tax. We have resolved our position concerning certain intercompany transactions with the tax authorities. Concerning the remaining issue, we anticipate it will become the subject ofcommenced litigation before the French tax courts in whichwhere the tax authorities will seek unpaid taxes, penalties, and interest.
In India, the tax authorities have issued notices of assessments to the Company seeking unpaid taxes and interest for the financial years covering 2013 to 2018 concerning our tax position with respect to certain corporate tax deductions and certain intercompany transactions. Some of these assessments remain in the audit phase where we are challenging them before the tax authorities while we are challenging some of the other assessments in the Indian tax courts.
The Company has recorded a net reserve for uncertain tax positions of $73.1$299.9 million and $134.6$315.6 million, including interest and penalties, in connection with its international audits at June 30, 20212022 and December 31, 2020,2021, respectively. The reserve balance at June 30, 2021 reflects the impact of current year settlement payments. In connection with our international tax audits, including in Australia and France, it is possible that we will incur material losses above the amounts reserved.
The Company’s major U.S. state taxing jurisdictions remain open from fiscal year 2013 through 2020, with several state audits currently in progress. The Company’s major international taxing jurisdictions remain open from 2012 through 2020.    2021.    
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Tax Court Proceedings
The Company's U.S. federal income tax returns for 2012 through 2014 had been subject to proceedings in U.S. Tax Court involving a dispute with the IRS regarding whether certain costs related to ANDAs were eligible to be expensed and deducted immediately or required to be amortized over longer periods. A trial was held in U.S. Tax Court in December 2018 and on April 27, 2021, the Court affirmed Mylan’s position and held that patent litigation expenses related to ANDAs are immediately deductible.
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The IRS has appealed this decision.
Accounting for Uncertainty in Income Taxes
The impact of an uncertain tax position that is more likely than not of being sustained upon audit by the relevant taxing authority must be recognized at the largest amount that is more likely than not to be sustained. No portion of an uncertain tax position will be recognized if the position has less than a 50% likelihood of being sustained.

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18.17.Litigation
The Company is involved in various disputes, governmental and/or regulatory inquiries, investigations and proceedings, tax proceedings and litigation matters, both in the U.S. and abroad, that arise from time to time, some of which could result in losses, including damages, fines and/or civil penalties, and/or criminal charges against the Company. These matters are often complex and have outcomes that are difficult to predict.
In addition, in connection with the Combination, the Company has generally assumed liability for, and control of, pending and threatened legal matters relating to the Upjohn Business – including certain matters initiated against Pfizer described below – and has agreed to indemnify Pfizer for liabilities arising out of such assumed legal matters. Pfizer, however, has agreed to retain various matters – including certain specified competition law matters – to the extent they arise from conduct during the pre-Distribution period and has agreed to indemnify the Company for liabilities arising out of such matters.
While the Company believes that it has meritorious defenses with respect to the claims asserted against it and the assumed legal matters referenced above, and intends to vigorously defend its position, the process of resolving these matters is inherently uncertain and may develop over a long period of time, and so it is not possible to predict the ultimate resolution of any such matter. It is possible that an unfavorable resolution of any of the ongoing matters could have a material effect on the Company’s business, financial condition, results of operations, cash flows, ability to pay dividends and/or stock price.
Some of these governmental inquiries, investigations, proceedings and litigation matters with which the Company is involved are described below, and unless otherwise disclosed, the Company is unable to predict the outcome of the matter or to provide an estimate of the range of reasonably possible material losses. The Company records accruals for loss contingencies to the extent we conclude it is probable that a liability has been incurred and the amount of the loss can be reasonably estimated. The Company is also involved in other pending proceedings for which, in the opinion of the Company based upon facts and circumstances known at the time, either the likelihood of loss is remote or any reasonably possible loss associated with the resolution of such proceedings is not expected to be material to the Company’s business, financial position, results of operations, cash flows, ability to pay dividends and/or stock price. If and when any reasonably possible losses associated with the resolution of such other pending proceedings, in the opinion of the Company, become material, the Company will disclose such matters.
Legal costs are recorded as incurred and are classified in SG&A in the Company’s condensed consolidated statements of operations.
EpiPen® Auto-Injector Litigation
The Company has beenand a former Mylan N.V. officer (collectively the “Mylan Defendants”) were named as a defendantdefendants in putative indirect purchaser class actions relating to the pricing and/or marketing of the EpiPen® Auto-Injector. The plaintiffs in these cases assertasserted violations of various federal and state antitrust and consumer protection laws, RICO as well as common law 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, as well as allegedly anti-competitive conduct. A former Mylan N.V. officer and other non-Viatris affiliated companies are also defendants in some of the class actions. Plaintiffs’ seeksought monetary damages, attorneys’ fees and costs. These lawsuits were filed in various federal and state courts and havewere either been dismissed or transferred into a MDL in the U.S. District Court for the District of Kansas and have been consolidated. The District Court certified anconsolidated or centralized. An antitrust class that applies to 17consisting of certain states and a RICO class.was ultimately certified. On June 23, 2021, the Court granted – in substantial part –the Company’s and former– the Mylan N.V. officer’sDefendants’ motion for summary judgment by dismissing certain antitrust claims and the RICO claims, which included RICO claims asserted against the former Mylan N.V. officer. Plaintiffs filed a motionIn February 2022, the parties reached an agreement to fully resolve this matter for reconsideration$264 million, which was accrued for during the year ended December 31, 2021. During the first quarter of 2022, $5.0 million of the summary judgment decisionsettlement was paid with respect to the RICO claims. On July 8, 2021, the Company filed a motion to decertify the class action with respect to the remaining antitrust claims. A trialamount of the settlement being paid in July 2022. The settlement was approved by the Court on July 11, 2022 and contains an express provision disclaiming and denying any wrongdoing or liability by the remaining antitrust claims against the Company is currently scheduled to begin on January 24, 2022.

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Mylan Defendants.
On February 14, 2020, the Company, together with other non-Viatris affiliated companies, were named as defendants in a putative direct purchaser class action filed in the U.S. District Court for the District of Kansas relating to the pricing and/or marketing of the EpiPen® Auto-Injector. The plaintiff in this case assertsOn September 21, 2021, after Plaintiffs’ then operative complaint was dismissed with an option to file a limited amended complaint, Plaintiffs filed an amended complaint asserting federal antitrust claims which are based on allegations that are similar to those inconcerning a patent settlement between Pfizer and Teva and other alleged actions regarding the putative indirect purchaser class actions discussed above. On November 3, 2020, the plaintiff filed a second amended complaint that is substantially similar to the allegations in the amended complaint.launch of Teva’s generic epinephrine auto-injector. Plaintiffs’ seek monetary damages, declaratory relief, attorneys’ fees and costs. On July 26, 2021, the Court dismissed the second amended complaint with an option for Plaintiff



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Beginning in March 2020, the Company, together with other non-Viatris affiliated companies, were named as defendants in putative direct purchaser class actions filed in the U.S. District Court for the District of Minnesota relating to contracts with certain pharmacy benefit managers concerning EpiPen® Auto-Injector. The plaintiffs claim that the alleged conduct resulted in the exclusion or restriction of competing products and the elimination of pricing constraints in violation of RICO and federal antitrust law. These actions have been consolidated. Plaintiffs’ seek monetary damages, attorneys’ fees and costs.
On April 24, 2017, Sanofi Aventis U.S., LLC (“Sanofi”) filed a lawsuit against the Company in the U.S. District Court for the District of New Jersey. This lawsuit has been transferred into the aforementioned MDL and alleges exclusive dealing and anti-competitive marketing practices in violation of the antitrust laws in connection with the sale and marketing of the EpiPen® Auto-Injector. Sanofi seeks monetary damages, declaratory relief, attorneys’ fees and costs. The Court granted the Company’s motion for summary judgment and dismissed Sanofi’s claims. Sanofi’s appeal is pending.was denied.
The Company has a total accrual of approximately $10.0$269.0 million related to this matterthese matters at June 30, 2021,2022, which is included in other current liabilities in the condensed consolidated balance sheets. Subsequent to June 30, 2022, the accrual has been reduced to $10.0 million as a result of the settlement payment discussed above. Although it is reasonably possible that the Company may incur additional losses from these matters, any amount cannot be reasonably estimated at this time. In addition, the Company expects to incur additional legal and other professional service expenses associated with such 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, financial condition, results of operations, cash flows, ability to pay dividends and/or stock price in future periods.
Drug Pricing Matters
Department of Justice
On December 3, 2015, the Company received a subpoena from the Antitrust Division of the DOJ seeking information relating to the marketing, pricing, and sale of certain of our generic products and any communications with competitors about such products. On September 8, 2016, the Company, as well as certain employees and a member of senior management, received subpoenas from the DOJ seeking similar information. Related search warrants also were executed.
On May 10, 2018, the Company received a civil investigative demand from the Civil Division of the DOJ seeking information relating to the pricing and sale of its generic drug products.
We are fully cooperating with these investigations, which we believe are related to a broader industry-wide investigation of the generic pharmaceutical industry.
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Civil Litigation
Beginning in 2016, the Company, along with other manufacturers, has been named as a defendant in lawsuits generally alleging anticompetitive conduct with respect to generic drugs. The lawsuits have been filed by plaintiffs, including putative classes of direct purchasers, indirect purchasers, and indirect resellers, as well as individual direct and indirect purchasers and certain cities and counties. They allege harm under federal and state laws, including federal and state antitrust laws, state consumer protection laws and unjust enrichment claims. Some of the lawsuits also name as defendants the Company’s President, including allegations against him with respect to a single drug product, and one of the Company’s sales employees, including allegations against him with respect to certain generic drugs. The vast majority of the lawsuits have been consolidated in an MDL proceeding in the Eastern District of Pennsylvania (“EDPA”). Plaintiffs generally seek monetary damages, restitution, declaratory and injunctive relief, attorneys’ fees and costs. The Court has ordered certain plaintiffs’ complaints regarding two single-drug product cases to proceed as bellwethers. The Company is named in those plaintiffs’ complaints that regard one of the two individual drug products.
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Attorneys General Litigation
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 and communications with competitors about such products. On December 14, 2016, attorneys general of certain states originally filed a complaint in the United States District Court for the District of Connecticut against several generic pharmaceutical drug manufacturers, including the Company, alleging anticompetitive conduct with respect to, among other things, a single drug product. The complaint has subsequently been amended, including on June 18, 2018, to add attorneys general alleging violations of federal and state antitrust laws, as well as violations of various states’ consumer protection laws. This lawsuit has been transferred to the aforementioned MDL proceeding in the EDPA. The operative complaint includes attorneys general of NaN states, the District of Columbia and the Commonwealth of Puerto Rico. The Company is alleged to have engaged in anticompetitive conduct with respect to four generic drug products. The amended complaint also includes claims asserted by attorneys general of NaN states and the Commonwealth of Puerto Rico against certain individuals, including the Company’s President, with respect to a single drug product. The amended complaint seeks declaratory and injunctive relief, disgorgement, attorneys’ fees and costs, and certain states seek monetary damages, civil penalties, restitution, and restitution.other equitable monetary relief. The States’ claim for disgorgement and restitution under federal law in this case has been dismissed.

On May 10, 2019, certain attorneys general filed a new complaint in the United States District Court for the District of Connecticut against various drug manufacturers and individuals, including the Company and one of its sales employees, alleging anticompetitive conduct with respect to additional generic drugs. On November 1, 2019, the complaint was amended, adding additional states as plaintiffs. The operative complaint is brought by attorneys general of NaN states, certain territories and the District of Columbia. The amended complaint also includes claims asserted by attorneys general of NaN states and certain territories against several individuals, including a Company sales employee. The amended complaint seeks declaratory and injunctive relief, disgorgement, attorneys’ fees and costs, and certain states seek monetary damages, civil penalties, restitution, and restitution.other equitable monetary relief. This lawsuit has been transferred to the aforementioned MDL proceeding in the EDPA.
On June 10, 2020, certain attorneys general of NaN states, certain territories and the District of Columbia filed a new complaint in the United States District Court for the District of Connecticut against drug manufacturers, including the Company, and individual defendants (none from the Company), alleging anticompetitive conduct with respect to additional generic drugs. On September 9, 2021, the complaint was amended, adding an additional state as a plaintiff. The operative complaint is brought by attorneys general of NaN states, certain territories and the District of Columbia. The amended complaint seeks declaratory and injunctive relief, disgorgement, attorneys’ fees and costs, and certain states seek monetary damages, civil penalties, restitution, and restitution.other equitable monetary relief. This lawsuit has been transferred to the aforementioned MDL proceeding in the EDPA. The courtEDPA and has been ordered that this caseto proceed as a bellwether.
Securities Related Litigation
Purported class action complaints were filed in October 2016 against Mylan N.V. and Mylan Inc. (collectively “Mylan”), certain of Mylan’s former directors and officers, and certain of the Company’s current directors and officers (collectively, for purposes of this paragraph, the “defendants”) in the United States District Court for the Southern District of New York (“SDNY”) on behalf of certain purchasers of securities of Mylan on the NASDAQ. The complaints alleged 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 the classification of their EpiPen® Auto-Injector as a non-innovator drug for purposes of the Medicaid Drug Rebate Program. On March 20, 2017, a consolidated amended complaint was filed alleging
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substantially similar claims, 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.
The operative complaint is the third amended consolidated complaint, which was filed on June 17, 2019, and contains the allegations as described above against Mylan, certain of Mylan’s former directors and officers, and certain of the Company’s current directors, officers, and employees (collectively, for purposes of this paragraph, the “defendants”). A class has been certified covering all persons or entities that purchased Mylan common stock between February 21, 2012 and May 24, 2019 excluding defendants, certain of the Company’s current directors and officers, former directors and officers of Mylan, members of their immediate families and their legal representatives, heirs, successors or assigns, and any entity in which defendants have or had a controlling interest. Plaintiffs seek damages and costs and expenses, including attorneys’ fees and expert costs. A decision on Defendants’ motion for summary judgment seeking to dismiss the case in its entirety and Plaintiffs’ cross-motion for partial summary judgment as to portions of certain claims is pending.
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
On April 30, 2017, a similar lawsuit was filed in the Tel Aviv District Court (Economic Division) in Israel, which has been stayed pending a decision in the SDNY class action litigation.
On February 26, 2019, MYL Litigation Recovery I LLC (“MYL Plaintiff”) (an assignee of entities that purportedly purchased stock of Mylan N.V.) filed an additional complaint in the SDNY against Mylan, certain of Mylan’s former officers and directors, and an officer of the Company asserting allegations pertaining to EpiPen® Auto-Injector under the federal securities laws that overlap in part with those asserted in the third amended complaint identified above. MYL Plaintiff’s complaint seeks monetary damages as well as the plaintiff’s costs. On May 6, 2020, MYL Plaintiff filed an amended complaint including additional allegations in connection with purportedly anticompetitive conduct with respect to EpiPen® Auto-Injector.
MYL Plaintiff subsequently filed a summons on October 30, 2020, naming Mylan, certain of Mylan’s former officers and directors, and certain of the Company’s current officers, directors, and employees in New York State Court, County of New York, claiming investment losses suffered as a result of purportedly false and misleading statements in connection with allegedly anticompetitive conduct concerning generic pharmaceuticals. Plaintiff is seeking monetary and punitive damages, attorneys’ fees and costs. The parties have resolved both matters filed by MYL Plaintiff and they have been dismissed with prejudice.
On February 14, 2020, the Abu Dhabi Investment Authority filed a complaint against Mylan in the SDNY asserting allegations pertaining to EpiPen® Auto-Injector and certain generic drugs under the federal securities laws that overlap with those asserted in the third amended complaint identified above. The Abu Dhabi Investment Authority’s complaint seeks monetary damages as well as the plaintiff’s fees and costs.
On June 26, 2020, a putative class action complaint was filed by the Public Employees Retirement System of Mississippi, which was subsequently amended on November 13, 2020, against Mylan N.V., certain of Mylan N.V.’s former directors and officers, and an officer and director of the Company (collectively for the purposes of this paragraph, the “defendants”) in the U.S. District Court for the Western District of Pennsylvania on behalf of certain purchasers of securities of Mylan N.V. The amended complaint alleges 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 the Morgantown manufacturing plant and inspections at the plant by the FDA. Plaintiff seeks certification of a class of purchasers of Mylan N.V. securities between February 16, 2016 and May 7, 2019. The complaint seeks monetary damages, as well as the plaintiff’s fees and costs.
On February 15, 2021, a complaint was filed by Skandia Mutual Life Ins. Co., Lansforsakringar AB, KBC Asset Management N.V., and GIC Private Limited, against the Company, certain of Mylan N.V.’s former directors and officers, a current director and officer of the Company, and current employees of the Company. The Complaint asserts claims which are based on allegations that are similar to those in the SDNY and the Western District of Pennsylvania complaints identified above. Plaintiffs seek compensatory damages, costs and expenses and attorneys’ fees.
On October 28, 2021, the Company and certain of its officers and directors were named as defendants in a putative class action lawsuit filed in the Court of Common Pleas of Allegheny County, Pennsylvania on behalf of former Mylan shareholders who received Company common stock in connection with the Combination. A non-Viatris affiliated company and persons were also named as defendants. The complaint alleges violations of Sections 11, 12(a)(2), and 15 of the Securities Act of 1933 for purportedly failing to disclose or misrepresenting material information in the registration statement and related prospectus issued in connection with the Combination. Plaintiffs seek monetary damages, reasonable costs and expenses, and certain other equitable and injunctive relief.
Opioids
The Company, along with other manufacturers, distributors, pharmacies, pharmacy benefit managers, and individual healthcare providers is a defendant in more than 1,000 cases in the United States and Canada filed by various plaintiffs, including counties, cities and other local governmental entities, asserting civil claims related to sales, marketing and/or
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Notes to Condensed Consolidated Financial Statements (Unaudited) - Continued
distribution practices with respect to prescription opioid products. In addition, lawsuits have been filed as putative class actions including on behalf of children with Neonatal Abstinence Syndrome due to alleged exposure to opioids.
The lawsuits generally seek equitable relief and monetary damages (including punitive and/or exemplary damages) based on a variety of legal theories, including various statutory and/or common law claims, such as negligence, public nuisance and unjust enrichment. The vast majority of these lawsuits have been consolidated in an MDL in the U.S. District Court for the Northern District Court of Ohio.
In November 2019,A liability-only trial has been ordered to take place by April 2023 in a coordinated proceeding in West Virginia state court involving the Company received a subpoena from the New York Department of Financial Services as part of an industry-wide inquiry into the effect of opioid prescriptions on New York health insurance premiums. The Company is fully cooperating with this subpoena request.
European Commission Proceedings
Perindopril
On July 9, 2014, the Commission issued a decision finding that the Company as well as several other companies, had violated EU competition rules relating to the product Perindopril and fined the Company approximately €17.2 million. The Company paid approximately $21.7 million related to this matter during the fourth quarter of 2014. The decision was affirmed on appeal by the General Court of the EU and is now on appeal to the CJEU. The Company has received a notice from an organization representing health insurers in the Netherlands stating an intention to commence follow-on litigation and asserting monetary damages.
Citalopram
On June 19, 2013, the Commission issued a decision finding that the Company as well as several other companies, had violated EU competition rules relating to the product Citalopram and fined the Company approximately €7.8 million, jointly and severally with Merck KGaA. The decision was affirmed on appeal by the General Court of the EU and the CJEU. The Commission’s matter as to the Company is now closed. The Company has received notices from European NHS and health insurers stating an intention to commence follow-on litigation and asserting monetary damages. The NHS England and Wales has instituted litigation against all parties to the Commission’s decision, including the Company.
The Company has also sought indemnification from Merck KGaA with respect to the €7.8 million portion of the fine for which Merck KGaA and the Company were held jointly and severally liable. Merck KGaA has counterclaimed against the Company seeking the same indemnification. In June 2018, the Frankfurt Regional Court issued a judgment ordering the Company to indemnify Merck KGaA with respect to the amount for which the parties were held jointly and severally liable. The Company has appealed this decision.
The Company has accrued approximately €11.2 million as of June 30, 2021 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.
U.K. Competition and Markets Authority
Paroxetine
On August 12, 2011, the Company received notice that the Office of Fair Trading (now the “CMA”) opened an investigation regarding possible infringement of the Competition Act 1998 and Articles 101 and 102 of the Treaty on the Functioning of the EU, with respect to alleged agreements related to Paroxetine. The CMA issued a decision on February 12, 2016, finding that the Company, Merck KGaA, and other companies were liable for infringing EUmanufacturers and U.K. competition rules. The CMA issued a penalty to Merck KGaA of approximately £5.8 million, for which the Company is jointly and severally liable for approximately £2.7 million. On appeal, the CAT affirmed the CMA’s decision but reduced the penalty to Merck KGaA to approximately £3.9 million, and reduced the amount for which the Company is jointly and severally liable to approximately £2.05 million.
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The Company has also received a notice from the NHS England and Wales stating an intention to commence follow- on litigation and asserting monetary damages.
The Company has accrued approximately £10.1 million as of June 30, 2021 related to this matter. It is reasonably possible that the Company 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.
Product Liability
Like other pharmaceutical companies, the Company is involved in a number of product liability lawsuits related to alleged personal injuries arising out of certain products manufactured/or distributed by the Company, including but not limited to those discussed below. Plaintiffs in these cases generally seek damages and other relief on various grounds for alleged personal injury and economic loss.
The Company has accrued approximately $103.1$73.9 million as of June 30, 20212022 for its product liability matters. 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.
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Nitrosamines
The Company, along with numerous other manufacturers, retailers, and others, are parties to litigation relating to alleged trace amounts of nitrosamine impurities in certain products, including valsartan and ranitidine. The vast majority of these lawsuits in the United States are pending in two MDLs, namely an MDL pending in the United States District Court for the District of New Jersey concerning valsartan and an MDL pending in the United States District Court for the Southern District of Florida concerning raniditine.ranitidine. The lawsuits against the Company in the MDLs include putative class actions seeking the refund of the purchase price and other economic and punitive damages allegedly sustained by consumers and end payors as well as individuals seeking compensatory and punitive damages for personal injuries allegedly caused by ingestion of the medications. Similar lawsuits pertaining to valsartan have been filed in Canada and other countries. Class certification motions are pending in the valsartan MDL. The Company has also received claims and inquiries related to these products, as well as requests to indemnify purchasers of the Company’s API and/ or finished dose forms of these products. The original master complaints concerning ranitidine were dismissed on December 31, 2020. The Company haswas not been named as a defendant in the amended master complaints, though it iswas still named in certain short form personal injury complaints. The end-payor plaintiffs and certain of the plaintiffs named in the short form personal injury complaints in the ranitidine matter have filed an appealappeals to the U.S. Court of Appeals for the Eleventh Circuit.

Lipitor
A number of individual and multi-plaintiff lawsuits have been filed against Pfizer in various federal and state courts alleging that the plaintiffs developed type 2 diabetes purportedly as a result of the ingestion of Lipitor. Plaintiffs seek compensatory and punitive damages. In February 2014, the federal actions were transferred for consolidated pre-trial proceedings to an MDL in the U.S. District Court for the District of South Carolina. Since 2016, certain cases in the MDL were remanded to certain state courts. In 2017, the District Court granted Pfizer’s motion for summary judgment, dismissing all of the cases pending in the MDL. In June 2018, this dismissal was affirmed by the U.S. Court of Appeals for the Fourth Circuit. The state court proceedings remain pending in various jurisdictions, including in California, Missouri, and New York. On January 27, 2021, the California Court granted Pfizer’s motion to exclude the opinions of plaintiffs’ only general causation expert in connection with his opinions involving the three lowest doses of Lipitor (10, 20 and 40 mg). The Company filed aCompany’s motion for summary judgment - which remains pending - in connection with the 10, 20, and 40 mg plaintiffs on June 7,was granted, resulting in their dismissal. On November 3, 2021, and Plaintiffs did not file an opposition.
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Viagra
Since April 2016, an MDL has been pending in the U.S. District Court for the Northern District of California, in which plaintiffs allege that they developed melanoma and/or the exacerbation of melanoma purportedly as a result of the ingestion of Viagra. Additional cases filed against Eli Lilly and Company (“Lilly”) with respect to Cialis have also been consolidated in the MDL. Plaintiffs seek compensatory and punitive damages. In January 2020, the District Court granted Pfizer’s and Lilly’s motion to exclude all of plaintiffs’ general causation opinions. As a result, in April 2020, the District Court entered summary judgment in favor of defendants and dismissed all of plaintiffs’ claims. In April 2020, plaintiffs filed a notice of appeal in the U.S. Court of Appeals for the Ninth Circuit. The parties have reached a settlement in principle.
Dilantin
Since 2018, a number of individual and multi-plaintiff lawsuits have been filed against Pfizer and related entities in various federal and state courts, alleging that the plaintiffs developed cerebellar atrophy as a result of the ingestion of Dilantin. Plaintiffs seek compensatory and punitive damages. The cases are in various stages, from the initial pleading stage to discovery, and some at the bellwether case selection phase. The parties have reached a settlement in principle.settled this matter.
Intellectual Property
The Company is involved in a number of patent litigation lawsuits involving the validity and/or infringement of patents held by branded pharmaceutical manufacturers including but not limited to the matters described below. The Company uses its business judgment to decide to market and sell certain products, in each case based on its belief that the applicable patents are invalid and/or that its products do not infringe, 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 3 times. Moreover, because of the discount pricing typically involved with bioequivalent products, patented branded products generally realize a substantially higher profit margin than generic and biosimilar products. The Company also faces challenges to its patents, including suits in various jurisdictions pursuant to which generic drug manufacturers, payers, governments, or other parties are seeking damages for allegedly causing delay of generic entry. An adverse decision in any of these matters could have an adverse effect that is material to our business, financial condition, results of operations, cash flows, ability to pay dividends and/or stock price.
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The Company has accrued approximately $302.5$192.7 million as of June 30, 20212022 for its intellectual property matters. 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.
Insulin Glargine
On October 24, 2017, Sanofi and affiliated entities (collectively for the purposes of this section, “Sanofi”), sued Mylan GmbH and other Mylan entities in the U.S. District Court for the District of New Jersey asserting that Mylan GmbH’s new drug application for insulin glargine injection 100 Units/mL vials and prefilled injection pens (SEMGLEE® vial and pens) infringed 18 U.S. patents. 2 of the 18 patents covered the insulin glargine formulation. Both of these patents have been held invalid and all appeals have concluded. These 2 patents were the only patents asserted against the SEMGLEE® vial product.
The 16 other asserted patents relate to a pen injection device (“device patents”) and were asserted only against the SEMGLEE® pen injection device. Prior to trial, Sanofi dismissed 12 of those device patents from the case and granted the Company a covenant not to sue with respect to them. On June 17, 2019, following the District Court’s claim construction order, the District Court entered judgment of non-infringement with respect to the asserted claims of 3 of the 4 remaining device patents (U.S. Patent Numbers 8,603,044, 8,679,069, 8,992,486).
Only one device patent remained for trial (U.S. Patent Number 9,526,844). On March 9, 2020, the District Court issued an opinion after trial finding all asserted claims of the ‘844 patent not infringed and invalid for lack of written description. Sanofi’s appeal is pending.
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On September 10, 2018, Mylan Pharmaceuticals Inc. (“MPI”) filed IPR petitions challenging 5 device patents (the ‘844, ‘044, ‘069, ‘486, and ‘008 patents). On April 2, 2020 and May 29, 2020, the PTAB issued final written decisions in the IPR proceedings finding all challenged claims unpatentable except for 2 claims of the ‘008 patent for which Sanofi granted the Company a covenant not to sue as described above. Sanofi’s appeals of all these IPR decisions are pending.
On March 26, 2021, the PTAB issued a final written decision in an IPR proceeding in which MPI challenged an additional Sanofi device patent (U.S. Patent Number RE47,614) and found all challenged claims unpatentable. Sanofi’s appeal is pending.
On June 11, 2020, the FDA approved the SEMGLEE® vial and pen products, which MPI began selling on August 31, 2020.
Dimethyl Fumarate
On June 30, 2017, Biogen MA Inc. and Biogen International GmbH (collectively, “Biogen”) sued MPI in the U.S. District Court for the Northern District of West Virginia asserting that MPI’s abbreviated new drug application for dimethyl fumarate delayed-release capsules containing 120 mg and 240 mg of dimethyl fumarate (generic for Tecfidera®) infringed 6six U.S. patents that Biogen had listed in the Orange Book: 6,509,376, 7,320,999, 7,619,001, 7,803,840, 8,759,393, and 8,399,514. All patents except for the ‘514 expired during the litigation and were dismissed from the case.
After a trial involving only the ’514 patent on June 18, 2020, the District Court issued a judgment finding all claims of the ’514 patent invalid for lack of adequate written description. On appeal, the Federal Circuit affirmed the District Court’s judgment.Biogen’s appealpetition for rehearing was denied.Biogen’s petition seeking review by the U.S. Supreme Court is pending.

On July 13, 2018, MPI filed an IPR petition challenging the ’514 patent based only on obviousness. On February 5, 2020, the PTAB issued a final written decision finding the claims not obvious. MPI’s appeal of the PTAB decision is pending.stayed pending resolution of Biogen’s request for U.S. Supreme Court review of the Federal Circuit’s affirmance of the District Court’s invalidity judgment.

On August 17, 2020, the FDA approved MPI’s dimethyl fumarate delayed-release capsules, which MPI began selling on August 18, 2020.
Lyrica - United Kingdom
Beginning in 2014, Pfizer was involved in patent litigation in the English courts concerning the validity of its Lyrica pain use patent. In 2015, the High Court of Justice in London ordered that the NHS England issue guidance for prescribers and pharmacists directing the prescription and dispensing of Lyrica by brand when pregabalin was prescribed for the treatment of neuropathic pain and entered a preliminary injunction against certain Sandoz group companies preventing the sale of Sandoz’s full label pregabalin product. Pfizer undertook to compensate certain generic companies and NHS entities for losses caused by these orders, which remained in effect until patent expiration in July 2017. In November 2018, the U.K. Supreme Court ruled that all the relevant claims directed to neuropathic pain were invalid.
Dr. Reddy’s Laboratories filed a claim for monetary damages, interest, and costs in May 2020, followed by the Scottish Ministers and fourteen Scottish Health Boards (together, NHS Scotland) in July 2020. In September 2020, Teva, Sandoz, Ranbaxy, Actavis, and the Secretary of State for Health and Social Care, together with 32 other NHS entities (together, NHS England, Wales, Scotland and Northern Ireland) filed their claims. The claimThe claims filed by Sandoz, Teva, Actavis, and Ranbaxy have been resolved. A trial on the remaining claims has been resolved and we have reached a settlement in principle to resolve the claim filed by Ranbaxy.
Lyrica - Canada
In June 2014, Pharmascience Inc. (“PMS”) commenced an action against Pfizer Canada Inc., Warner-Lambert Company and Warner-Lambert Company LLC (the Pfizer Canada Defendants) seeking damages in connection with an earlier unsuccessful patent litigation brought by the Pfizer Canada Defendants involving pregabalin. PMS claims lost profit damages fromset for November 30, 2010, the date it received tentative regulatory approval for its pregabalin product, to February 13, 2013, the date Pfizer’s patent case against PMS was dismissed. A trial that will take place intermittently over a few week period began on July 19, 2021.
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Other Litigation
The Company is involved in various other legal proceedings including commercial, contractual, employment, or other similar matters that are considered normal to its business. The Company has approximately $12.7$34.7 million accrued related to these various other legal proceedings at June 30, 2021.2022.

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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 Viatris Inc. and subsidiaries for the periods presented. Unless context requires otherwise, the “Company,” “Viatris,” “our” or “we” refer to Viatris Inc. 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 Viatris’ 20202021 Form 10-K, the unaudited interim financial statements and related Notes included in Part I — ITEM 1 of this Form 10-Q and our other SEC filings and public disclosures. The interim results of operations and comprehensive earningsloss for the three and six months ended June 30, 2021,2022, and cash flows for the six months ended June 30, 20212022 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 Biocon Biologics Transaction, the Combination, the benefits and synergies of the Combination or our global restructuring program, future opportunities for the Company and its products and any other statements regarding the Company’s future operations, financial or operating results, capital allocation, dividend policy and payments, debt ratio and covenants, anticipated business levels, future earnings, planned activities, anticipated growth, market opportunities, strategies, competitions, commitments, confidence in future results, efforts to create, enhance or otherwise unlock the value of our unique global platform, and other expectations and targets for future periods. Forward-looking statements may often be identified by the use of words such as “will”, “may”, “could”, “should”, “would”, “project”, “believe”, “anticipate”, “expect”, “plan”, “estimate”, “forecast”, “potential”, “pipeline”, “intend”, “continue”, “target”, “seek” 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:

the integration of Mylan and the Upjohn Business or the implementation of the Company’s global restructuring program being more difficult, time consuming or costly than expected;
the possibility that the Company may be unable to achieve expected benefits, synergies and operating efficiencies in connection with the Combination or its global restructuring program within the expected timeframe or at all;
the possibility that the Companypending Biocon Biologics Transaction and other strategic initiatives, including potential divestitures, may be unable to successfully integrate Mylan and the Upjohn Business or implement its global restructuring program;not achieve their intended benefits;
operational or financial difficulties or losses associated with the Company’s reliance on agreements with Pfizer in connection with the Combination, including with respect to transition services;
the possibility that the Company may be unable to achieve all intended benefits of its strategic initiatives;
the potential impact of public health outbreaks, epidemics and pandemics, including the ongoing challenges and uncertainties posed by the COVID-19 pandemic;
the Company’s failure to achieve expected or targeted future financial and operating performance and results;
actions and decisions of healthcare and pharmaceutical regulators;
changes in relevant laws and regulations, including but not limited to changes in tax, healthcare and pharmaceutical laws and regulations globally (including the impact of potential tax reform in the U.S.);
the ability to attract and retain key personnel;
the Company’s liquidity, capital resources and ability to obtain financing;
any regulatory, legal or other impediments to the Company’s ability to bring new products to market, including but not limited to “at-risk launches”;
success of clinical trials and the Company’s or its partners’ ability to execute on new product opportunities and develop, manufacture and commercialize products;
any changes in or difficulties with the Company’s manufacturing facilities, including with respect to inspections, remediation and restructuring activities, supply chain or inventory or the ability to meet anticipated demand;
the scope, timing and outcome of any ongoing legal proceedings, including government inquiries or investigations, and the impact of any such proceedings on the Company;
any significant breach of data security or data privacy or disruptions to our information technology systems;
risks associated with having significant operations globally;
the ability to protect intellectual property and preserve intellectual property rights;
changes in third-party relationships;
the effect of any changes in the Company’s or its partners’ customer and supplier relationships and customer purchasing patterns, including customer loss and business disruption being greater than expected following the Combination;
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the impacts of competition, including decreases in sales or revenues as a result of the loss of market exclusivity for certain products;
changes in the economic and financial conditions of the Company or its partners;
uncertainties regarding future demand, pricing and reimbursement for the Company’s products;
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uncertainties and matters beyond the control of management, including but not limited to general political and economic conditions, inflation rates and global exchange rates; 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 U.S. GAAP and related standards or on an adjusted basis.

For more detailed information on the risks and uncertainties associated with Viatris, see the risks described in Part I, Item 1A in the 20202021 Form 10-K, and our other filings with the SEC. You can access Viatris’ filings with the SEC through the SEC website at www.sec.gov or through our website, and Viatris strongly encourages you to do so. Viatris routinely posts information that may be important to investors on our website at investor.viatris.com, and we use this website address as a means of disclosing material information to the public in a broad, non-exclusionary manner for purposes of the SEC’s Regulation Fair Disclosure (Reg FD). The contents of our website are not incorporated by reference in this Form 10-Q and shall not be deemed “filed” under the Securities Exchange Act of 1934, as amended. Viatris undertakes no obligation to update any statements herein for revisions or changes after the filing date of this Form 10-Q other than as required by law.
Explanatory Note
In accordance with ASC 805, Business Combinations, Mylan is considered the accounting acquirer of the Upjohn Business and all historical financial information of the Company prior to November 16, 2020 represents Mylan’s historical results and the Company’s thereafter.
Company Overview
Viatris is a global healthcare company formed in November 2020 through the combination of Mylan and Upjohn, whose mission is to empower people worldwide to live healthier at every stage of life. By integrating the strengths of these two businesses, including our global workforce of more than 40,000 employees and contractors, Viatris aims to deliver increased access to affordable, quality medicines for patients worldwidelife, regardless of geography or circumstance. Viatris brings togetherImproving the ability of patients to gain access to sustainable and high-quality healthcare is our relentless pursuit. One that rests on visionary thinking, determination and best-in-class capabilities that were strategically built to remove barriers across the health spectrum and advance access globally.
Viatris’ seasoned management team is focused on ensuring that the Company is optimally structured and efficiently resourced to deliver sustainable value to patients, shareholders, customers and other stakeholders. With a global workforce of approximately 37,000, the Company has industry leading commercial, R&D, regulatory, manufacturing, legal and medical expertise complemented by a strong commitment to quality and unparalleled geographic footprint to deliver high-quality medicines to patients in more than 165 countries and territories. Viatris’ portfolio comprises more than 1,400 approved molecules across a wide range of keymore than 10 major therapeutic areas, including globally recognized iconic and key brand, generic,brands, generics, complex generic,generics, and biosimilar products. Viatrisbiosimilars. The Company operates approximately 5040 manufacturing sites worldwide that produce oral solid doses, injectables, complex dosage forms and APIs. Viatris is headquartered in the U.S., with global centers in Pittsburgh, Pennsylvania, Shanghai, China and Hyderabad, India.
Viatris has four reportable segments: Developed Markets, Greater China, JANZ, and Emerging Markets. The Company reports segment information on the basis of markets and geography. In conjunction with the formation of Viatris, the Company has changedgeography, which reflects its reportable segments, from North America, Europe, and Rest of World, to Developed Markets, Greater China, JANZ, and Emerging Markets. This approach reflects the Company’s focus on bringing its broad and diversified portfolio of branded, complex generics and biosimilars, and generic products to people in markets everywhere. Our Developed Markets segment comprises our operations primarily in North America and Europe. Our Greater China segment includes our operations in China, Taiwan and Hong Kong. Our JANZ segment reflects our operations in Japan, Australia and New Zealand. Our Emerging Markets segment encompasses our operationspresence in more than 125 countries with developing markets and emerging economies including countries in Asia, Africa, Eastern Europe, Latin America and the Middle East South and Central America, Africa and Eastern Europe, and also includesas well as the Company’s anti-retroviralARV franchise.
Certain Market and Industry Factors
The global pharmaceutical industry is a highly competitive and highly regulated industry. As a result, we face a number of industry-specific factors and challenges, which can significantly impact our results. The following discussion highlights some of these key factors and market conditions.
Generic products, particularly in the U.S., generally contribute most significantly to revenues and gross margins at the time of their launch, and 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
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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. Conversely, generic products generally experience less volatility over a longer period of time in Europe as compared to the U.S., primarily due to the role of government oversight of healthcare systems in the region.
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. For example, several companies launched a generic to Lyrica® in Japan in December 2020 despite pending patent infringement litigation. While the litigation remains ongoing, the rate
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Certain markets in which we do business outside of the U.S. 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.
Additionally, a number of markets in which we operate outside of the U.S. 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 priority placement 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 in certain countries.
Recent Developments
Dividend Reinvestment and Share Purchase Plan
On May 6, 2022, the Company announced that its Board of Directors had authorized a DRIP. The DRIP allows shareholders to automatically reinvest all or a portion of the cash dividends paid on their shares of the Company’s common stock and to make certain additional optional cash investments in the Company’s common stock.

International Operations
The ongoing conflict between Russia and Ukraine did not have a material impact on our business as the combined total revenues for both countries were less than 1% of consolidated total revenues during each of the three and six months ended June 30, 2022 and 2021. However, trade controls, sanctions, supply chain and staffing challenges and other economic considerations related to the conflict have impacted our operations in these markets and may negatively impact our financial results in future periods. In addition, a significant escalation or expansion of the conflict’s current scope may have a negative impact on our operations and financial results in future periods. For a further discussion of the risks we encounter in our business, including the risks of conducting our business internationally, please refer to Part I, Item 1A. Risk Factors in our 2021 Form 10-K.

Under ASC 830, Foreign Currency Matters (“ASC 830”), a highly inflationary economy is one that has cumulative inflation of approximately 100% or more over a three-year period. Effective April 1, 2022, we classified Turkey as highly inflationary. In accordance with ASC 830, starting with the second quarter of 2022, we began to utilize the U.S. dollar as our functional currency in Turkey, which historically utilized the Turkish lira as the functional currency. The impact of applying the guidance in ASC 830 did not have a material impact on our results of operations, comprehensive earnings, financial position, equity and cash flows for the three months ended June 30, 2022. The impacted net sales for the three months ended June 30, 2022 and total assets at June 30, 2022 represented less than 1% of our consolidated net sales and total assets, respectively.

Biocon Biologics Agreement
On February 27, 2022, the Company entered into an agreement to contribute its biosimilars portfolio to Biocon Biologics. Under the terms of the Biocon Agreement, at closing Viatris will receive an up-front cash payment of $2.0 billion, subject to certain adjustments, ownership of at least 12.9% of Biocon Biologics, on a fully diluted basis, in the form of convertible preferred equity which will have certain priority rights with respect to certain liquidity events, and $335 million as additional cash payments that are expected to be paid in 2024. Upon closing of the transaction, we expect to record a gain for the difference between the consideration received, including the fair value of the convertible preferred equity, and the carrying value of the biosimilars portfolio. The companies will also enter into a two-year transition services agreement, subject to extension in certain circumstances, during which time Viatris will provide certain commercial and administrative services for an applicable service fee. The transaction is expected to close in the second half of 2022 and is subject to various closing conditions (including regulatory approvals).

Share Repurchase Program
On February 28, 2022, the Company announced that its Board of Directors had authorized a share repurchase program for the repurchase of up to $1.0 billion of the Company’s shares of common stock. The Company has not yet repurchased any
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Recent Developmentsshares of common stock under the share repurchase program and the share repurchase program does not obligate the Company to acquire any particular amount of common stock.
SEMGLEE®Cyclosporine Ophthalmic Emulsion
On June 11, 2020,February 3, 2022, the Company announced that it had received approval from the FDA approved the SEMGLEE® vial and pen products, which the Company began selling on August 31, 2020. On July 28, 2021, Viatris and Biocon Biologics Ltd. announced that the FDA had approved SEMGLEE® (insulin glargine-yfgn) injection asfor its ANDA for Cyclosporine Ophthalmic Emulsion 0.05%, the first interchangeable biosimilar product under the 351(k) regulatory pathway.generic version of Allergan's Restasis®. Cyclosporine Ophthalmic Emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca, also known as dry eye. The interchangeable SEMGLEE® product, which will allow substitution of SEMGLEE® for the reference product, Lantus®, at the pharmacy counter, will be introduced before the endcommercial launch of the year. The Company is eligible to have exclusivity for 12 months before the FDA can approve another biosimilar interchangeable to Lantus®. Commercial preparations for launch are underway. Over the next few months, Viatris will transition the current product to the 351(k) interchangeable product.occurred in February 2022.
2020 Restructuring Program
During the fourth quarter of 2020, Viatris announced a significant global restructuring program in order to achieve synergies and ensure that the organization is optimally structured and efficiently resourced to deliver sustainable value to patients, shareholders, customers, and other stakeholders. Viatris’ restructuring initiative incorporates and expands onAs part of the restructuring, program announced by Mylan N.V. earlier in 2020 as part of its business transformation efforts. Thethe Company expects to optimizeis optimizing its commercial capabilities and enabling functions, and close, downsizeclosing, downsizing or divest up to 15divesting certain manufacturing facilities globally that are deemed to be no longer viable either due to surplus capacity, challenging market dynamics or a shift in its product portfolio toward more complex products. As a result, Viatris expects that up to 20% of its global workforce may be impacted upon completion of the restructuring initiative.
For the committed restructuring actions, the Company expects to incur total pre-tax charges ranging between $1.1 billion andof up to approximately $1.4 billion. Such charges are expected to include between $350 million andup to approximately $450 million of non-cash charges mainly related to accelerated depreciation and asset impairment charges, including inventory write-offs. The remaining estimated cash costs of between $750 million andup to approximately $950 million are expected to be primarily related to severance and employee benefits expense, as well as other costs, including those related to contract terminations and decommissioningother plant disposal costs. In addition, management believes the potential annual savings related to these committed restructuring activities to be between $700 million andup to approximately $900 million once fully implemented, with most of these savings expected to improve operating cash flow.
During the three and six months ended June 30, 2021, the Company recorded pre-tax charges of $251.9 million and $565.5 million, respectively. For the charges recognized during the three months ended June 30, 2021, $80.8 million were non-cash asset impairment charges and the remaining charges were primarily related to severance and employee benefits. Included within the charges during the six months ended June 30, 2021 were $231.8 million for non-cash asset impairment charges with the remaining charges primarily related to severance and employee benefits.
Impact of the Coronavirus pandemic on our business and results of operationsPandemic
As a leading global pharmaceutical company, Viatris is committed to continue doing its part in support of public health needs amid the evolving COVID-19 pandemic. The Company’s priorities remain protecting the health and safety of our workforce, continuing to produce critically needed medicines, deploying resources and expertise in the fight against COVID-19 through potential prevention and treatment efforts, supporting the communities in which we operate and maintaining the health of our overall business.
The following section discusses the important measures the Company continues to take in light of the COVID-19 pandemic.

Employee Health and Safety

Viatris continues to align with government and health authority guidelines in an effort to safeguard our workforce and continues to make assessments on an ongoing basis.

While Viatris’ business operations are currently considered essential based on government guidelines throughout the world due to the important role pharmaceutical manufacturers play within the global healthcare system, As a result, many Viatris administrative offices continue operating under work from home protocols.
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Because protecting the health and safety of our workforce remains paramount, Viatris has taken extra precautions at manufacturing facilities to aid in the protection of site personnel and operations, including the implementation of social distancing guidelines, daily health assessments and split shifts where feasible.

Many customer facing field personnel have moved tocontinue on a remote engagement model to ensure continued support for healthcare professionals, patient care and access to needed products.

Global restrictions have been placed on travel and in-person meetings.

Viatris has taken steps to protect the safety of study participants, our employees and staff at clinical trial sites and ensure regulatory compliance and scientific integrity of trial data.

Continuing to Produce Critically Needed Medicines
Manufacturing and Supply

Viatris has activated worldwide business continuity plans to seek to ensure that our global supply chain platform continues to operate without significant disruption.

All Additionally, all of our manufacturing facilities, and those of our key global partners, are currently operational and, at this time, we are not experiencing any significant disruptions to our supply chain, including the availability of APIs. Also, we are currently not experiencing any negative impact on our customer service levels.

Viatris has a broad, diverse and resilient global manufacturing and supply chain footprint. We are not dependent on any one country or site. Even in India, our manufacturing footprint is spread over five different states, which mitigates the risk of disruption in any given part of the country.

Viatris continues to engage with regulatory authorities around the world who are committed to maintaining ongoing regulatory processes while also continuing to make available our global R&D, regulatory and manufacturing expertise and capacity to partners who may be in need of additional resources.

Commercial Operations

We have and continue to experience fluctuations in demand trends due to COVID-19. We will continue to monitor trends closely as we work to ensure patients have access to needed medicine.

Inventorydisruptions. Current inventory levels, both ours and those in our distribution channel, remain in-line with normal levels and are currently assessed to be sufficient for anticipated demand.levels.

Deploying Resources and Expertise in the Fight Against COVID-19
Product Development

On May 12, 2020, Mylan announced a global collaboration with Gilead Sciences, Inc. to expand access to the investigational antiviral remdesivir for the potential treatment of COVID-19. Under the terms of the license agreement the Company has rights to manufacture and distribute remdesivir in 127 low-and middle-income countries, including India.

On July 6, 2020, Mylan announced that the DCGI approved its remdesivir 100 mg/vial for restricted emergency use in India as part of the DCGI’s accelerated approval process to address urgent, unmet needs amid the evolving COVID-19 pandemic.

On November 20, 2020, the World Health Organization issued a conditional recommendation against the use of remdesivir in hospitalized patients, regardless of disease severity, as there was no evidence that remdesivir improved survival and other outcomes in these patients.
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Viatris has ramped up production of antiviral medicines, including remdesivir and ambisome, and continues to work with government authorities in India to further reduce the cost of the medicines and educate more than 20,000 healthcare professionals about product usage.
Maintaining the Health of Our Overall Business

Access to Capital Markets and Liquidity

While currently we are not experiencing any negative liquidity trends related to the COVID-19 pandemic, we continue to closely monitor developments and the potential negative impact on our operating performance and our ability to access the capital markets.

Due to the Company’s ability to generate significant cash flows from operations, as well as its revolving credit agreement, other short-term borrowing facilities and access to capital markets, we believe that we currently have, and will maintain, the ability to meet foreseeable liquidity needs.

Impact on Results of Operations

The global spread of COVID-19 has created and continues to create significant volatility, uncertainty and economic disruption affecting the markets we serve.serve, including impacts on supply chain partners, third-party manufacturers, logistics providers and other vendors. The extent to which the COVID-19 pandemic will impact our business, operations and financial results in future periods will depend on numerous evolving factors that are beyond our control and that we may not be able to accurately predict. For additional information, see “Item 2. Management’s Discussionpredict, and Analysiscould adversely impact our results of Financial Conditionoperations in future periods. Due to the Company’s ability to generate significant cash flows from operations, combined with our access to borrowing facilities and Results of Operations.capital markets, we believe that we currently have, and will maintain, the ability to meet foreseeable liquidity needs.

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Financial Summary
The table below is a summary of the Company’s financial results for the three and six months ended June 30, 20212022 compared to the prior year period:
Three Months Ended
June 30,
(In millions, except per share amounts)20212020Change% Change
Total revenues$4,577.8 $2,731.2 $1,846.6 68 %
Gross profit1,327.7 1,025.7 302.0 29 %
(Loss) earnings from operations(47.8)134.2 (182.0)(136)%
Net (loss) earnings(279.2)39.4 (318.6)nm
Diluted (loss) earnings per share$(0.23)$0.08 $(0.31)nm
Six Months Ended
June 30,
(In millions, except per share amounts)20212020Change% Change
Total revenues$9,008.1 $5,350.4 $3,657.7 68 %
Gross profit2,455.0 1,931.8 523.2 27 %
(Loss) earnings from operations(314.0)318.9 (632.9)(198)%
Net (loss) earnings(1,316.8)60.2 (1,377.0)nm
Diluted (loss) earnings per share$(1.09)$0.12 $(1.21)nm

Three Months Ended
June 30,
(In millions, except per share amounts and %s)20222021Change
Total revenues$4,116.8 $4,577.8 $(461.0)
Gross profit1,703.3 1,327.7 375.6 
Earnings (loss) from operations548.7 (47.8)596.5 
Net earnings (loss)313.9 (279.2)593.1 
Diluted earnings (loss) per share$0.26 $(0.23)$0.49 
Six Months Ended
June 30,
(In millions, except per share amounts and %s)20222021Change
Total revenues$8,308.5 $9,008.1 $(699.6)
Gross profit3,474.5 2,455.0 1,019.5 
Earnings (loss) from operations1,256.1 (314.0)1,570.1 
Net earnings (loss)713.1 (1,316.8)2,029.9 
Diluted earnings (loss) per share$0.59 $(1.09)$1.68 
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 measures of “constant currency” net sales and total revenues. These measures provide information on the change in net sales and total revenues 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 net sales and total revenues 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.
More information about non-GAAP measures used by the Company as part of this discussion, including adjusted cost of sales, adjusted gross margins, adjusted net earnings and adjusted EBITDA (all of which are defined below) can be found in “Item 2. Management’s Discussion and Analysis of Financial Condition and- Results of Operations -and Results of Operations - Use of Non-GAAP Financial Measures.

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Results of Operations
Three Months Ended June 30, 20212022 Compared to Three Months Ended June 30, 20202021
Three Months EndedThree Months Ended
June 30,June 30,
(In millions, except %s)(In millions, except %s)20212020% Change
2021 Currency Impact (1)
2021 Constant Currency Revenues
Constant Currency % Change (2)
(In millions, except %s)20222021% Change
2022 Currency Impact (1)
2022 Constant Currency Revenues
Constant Currency % Change (2)
Net salesNet salesNet sales
Developed MarketsDeveloped Markets$2,640.4 $1,982.7 33 %$(112.1)$2,528.3 28 %Developed Markets$2,479.1 $2,640.4 (6)%$181.4 $2,660.5 %
Greater ChinaGreater China550.3 22.7 nm(0.5)549.8 nmGreater China548.3 550.3 — %5.4 553.7 %
JANZJANZ501.0 280.2 79 %(14.9)486.1 73 %JANZ427.1 501.0 (15)%64.9 491.9 (2)%
Emerging MarketsEmerging Markets870.0 410.3 112 %(24.3)845.7 106 %Emerging Markets650.9 870.0 (25)%54.0 705.0 (19)%
Total net salesTotal net sales$4,561.7 $2,695.9 69 %$(151.8)$4,409.9 64 %Total net sales$4,105.4 $4,561.7 (10)%$305.7 $4,411.1 (3)%
Other revenues (3)
Other revenues (3)
16.1 35.3 (54)%(0.8)15.3 (57)%
Other revenues (3)
11.4 16.1 (29)%0.8 12.2 (24)%
Consolidated total revenues (4)
Consolidated total revenues (4)
$4,577.8 $2,731.2 68 %$(152.6)$4,425.2 62 %
Consolidated total revenues (4)
$4,116.8 $4,577.8 (10)%$306.5 $4,423.3 (3)%
____________
(1)Currency impact is shown as unfavorable (favorable).
(2)The constant currency percentage change is derived by translating net sales or revenues for the current period at prior year comparative period exchange rates, and in doing so shows the percentage change from 20212022 constant currency net sales or revenues to the corresponding amount in the prior year.
(3)For the three months ended June 30, 2021,2022, other revenues in Developed Markets Greater China, JANZ, and Emerging Markets were approximately $12.2 million, $(1.4) million, $0.6$4.8 million and $4.7$6.6 million, respectively.
(4)Amounts exclude intersegment revenue thatwhich eliminates on a consolidated basis.
Total Revenues
For the current quarter, Viatris reported total revenues of $4.58$4.12 billion, compared to $2.73$4.58 billion for the comparable prior year period, representing an increasea decrease of $1.85 billion,$461.0 million, or 68%10%. Total revenues include both net sales and other revenues from third parties. Net sales for the current quarter were $4.56$4.11 billion, compared to $2.70$4.56 billion for the comparable prior year period, representing an increasea decrease of $1.87 billion,$456.3 million, or 69%10%. Other revenues for the current quarter were $16.1$11.4 million, compared to $35.3$16.1 million for the comparable prior year period.
The increasedecrease in total revenues and net sales was primarily driven by net sales totaling $1.63 billion from the Upjohn Business in the current quarter and approximately $223.9 million of new product sales, partially offset by a decrease of approximately $139.2 million in net sales from existing products, primarily as a result of lower pricing. New product sales include new products launched in 2021 and the carryoverunfavorable impact of new products, including business development, launched since July 1, 2020. The Company’s net sales were favorably impacted by the effect of foreign currency translation of approximately $305.7 million, or 7%, primarily reflecting changes in the U.S. Dollar as compared to the currencies of subsidiaries in countries within the EU and in India and Australia. The net favorable impact of foreign currency translation on net sales was approximately $151.8 million, or 6%.Japan. On a constant currency basis, the increasedecrease in net sales was approximately $1.71 billion,$150.6 million, or 64%3% for the three months ended June 30, 2021. We estimate that the COVID-19 pandemic positively impacted our second quarter 20212022. This decrease was due to competition on certain key U.S. products representing a decline of approximately $70 million and approximately $164 million as a result of other base business erosion. The decrease in net sales from existing products was partially offset by approximately 4%, primarily driven by the partial recovery$83.8 million of customer buying patterns in Europe and certainnew product sales. New product sales include new products launched in India during2022 and the second quartercarryover impact of 2021 as compared tonew products, including business development, launched within the prior year period. The prior year period was negatively impacted by the reversal of forward purchasing patterns that occurred in the first quarter of 2020.last twelve months.

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, seasonality, and the amount, if any, of additional competition in the market. Our top ten products in terms of net sales, in the aggregate, represented approximately 33%34% and 26%33% for the three months ended June 30, 2022 and 2021, and 2020, respectively, with the year-over-year increase a result of the Combination. This percentage may fluctuate based upon the timing of new product launches, seasonality and the timing of changes in competition.respectively.
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Net sales are derived from our four reporting segments: Developed Markets, Greater China, JANZ, and Emerging Markets.
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Developed Markets Segment

Net sales from Developed Markets increaseddecreased by $657.7$161.3 million or 33%6% during the three months ended June 30, 20212022 when compared to the prior year period. This decrease was due primarily to the unfavorable impact of foreign currency translation of approximately $181.4 million, or 7%. Constant currency net sales increased by approximately $20.1 million, or 1% when compared to the prior year period. Net sales within North America totaled approximately $1.20$1.10 billion and net sales within Europe totaled approximately $1.44$1.38 billion. ThisThe increase was due primarily to net sales from the Upjohn Business in the current quarter of $519.7 million anddriven by new product sales, including Insulin Glargine and Semglee® in the portfolioU.S., and higher volumes of thrombosisexisting products in Europe acquired from Aspen inEurope. These increases were partially offset by lower net sales of certain key products within the fourth quarter of 2020, as well as higher volumes in Europe as compared to the prior year period due to the higher COVID-19 impact during the second quarter of 2020U.S., including Miacalcin® and Perforomist®, as a result of customer buying patterns, and Yulperi growth in North America. This increase was partially offset by lower pricing in Europe, and lower pricing and volumes on net sales of certain existing North American products, including Wixela, Xulane, and Perforomist, primarily driven by additional competition. Lower volumes were also due to the impact of product divestitures, including certain North American OTC products during the current quarter and other products during 2020 as a result of the Combination. The favorable impact of foreign currency translation on current period net sales, primarily in Europe, was approximately $112.1 million, or 6%. Constant currency net sales increased by approximately $545.6 million, or 28% when compared to the prior year period.

Greater China Segment
Net sales from Greater China increaseddecreased by $527.6$2.0 million or less than 1% for the three months ended June 30, 20212022 when compared to the prior year period. This increasedecrease was primarily the result of net sales from the Upjohn Business in the current quarterunfavorable impact of $540.6 million. This increase was partially offset by lower net sales of existing products, driven by lower volumes, which were negatively impacted by competitive market conditions, including VBP.foreign currency translation. The favorableunfavorable impact of foreign currency translation was approximately $0.5$5.4 million, or 2%1%. Constant currency net sales increased by approximately $527.1$3.4 million or 1% when compared to the prior year.
JANZ Segment
Net sales from JANZ increaseddecreased by $220.8$73.9 million or 79%15% for the three months ended June 30, 20212022 when compared to the prior year period. This increasedecrease was primarily the result of net sales from the Upjohn Business in the current quarter of $191.9 million and higher net sales of existing products driven by higher volumes in Japan primarily related to theunfavorable impact of the termination of the collaboration arrangement with Pfizer in the prior year, partially offset by lower pricing in Australia driven by government price reductions and product competition. Foreignforeign currency translation had a favorable impact of approximately $14.9$64.9 million, or 5%13%. Constant currency net sales increaseddecreased by approximately $205.9$9.0 million, or 74%2% when compared to the prior year period. The decrease was primarily due to lower net sales of existing products mainly driven by lower pricing in Japan as a result of government price reductions and additional competition. This decrease was partially offset by higher volumes on net sales of existing products in Japan, including for Celebrex®.
Emerging Markets Segment
Net sales from Emerging Markets increaseddecreased by $459.7$219.1 million or 112%25% for the three months ended June 30, 20212022 when compared to the prior year period. This increasedecrease was the resultmainly driven by lower volumes of net sales from the Upjohn Business in the current quarter of $377.1 million and COVID-19 related product salesproducts in India, primarily related to remdesivir and ambisome. This increase was partially offset byambisome, and lower volumes and pricingsales of antiretroviral drugsARV products as a result of competitive market conditions. The decrease was further driven by the timingunfavorable impact of orders across multiple markets, and lowerforeign currency translation. These decreases were partially offset by higher volumes in other markets.certain markets in the segment. The favorableunfavorable impact of foreign currency translation was $24.3$54.0 million or 6%. Constant currency net sales increaseddecreased by approximately $435.4$165.1 million, or 106%19%.
Cost of Sales and Gross Profit
Cost of sales increaseddecreased from $1.71 billion for the three months ended June 30, 2020 to $3.25 billion for the three months ended June 30, 2021.2021 to $2.41 billion for the three months ended June 30, 2022. Cost of sales was primarily impacted by purchase accounting related amortization of the fair value of step-up of acquired intangible assetsinventory of $477.3 million in the comparable prior year period, lower restructuring costs in the current period related to the 2020 restructuring program versus the comparable prior year period, and lower costs associated with other special items, which are described further in the section titled Use of Non-GAAP Financial Measures.
Gross profit for the three months ended June 30, 2022 was $1.70 billion and gross margins were 41%. For the three months ended June 30, 2021, gross profit was $1.33 billion and gross margins were 29%. ForThis change is primarily related to the three months ended June 30, 2020, gross profit was $1.03 billion anddecrease in cost of sales. Adjusted gross margins were 38%. Cost of sales from the Upjohn Business, including the impact of amortization expense, was $1.24 billion59% for the three months ended June 30, 2021. This includes increased amortization expense of $778.0 million primarily for purchase accounting related amortization of intangible assets and the step-up of acquired inventory. Gross profit from net sales of existing products was impacted equally by lower volumes and lower pricing. Adjusted gross margins were 58% for2022, essentially flat when compared to the three months ended June 30, 2021, compared to 54% for the three months ended June 30, 2020, with the year-over-year increase driven by the impact of the Combination.2021.
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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 June 30, 20212022 compared to the three months ended June 30, 20202021 is as follows:
Three Months EndedThree Months Ended
June 30,June 30,
(In millions, except %s)(In millions, except %s)20212020(In millions, except %s)20222021
U.S. GAAP cost of salesU.S. GAAP cost of sales$3,250.1 $1,705.5 U.S. GAAP cost of sales$2,413.5 $3,250.1 
Deduct:Deduct:Deduct:
Purchase accounting related amortizationPurchase accounting related amortization(1,169.8)(351.8)Purchase accounting related amortization(644.9)(1,169.8)
Acquisition related itemsAcquisition related items(1.0)(1.3)Acquisition related items(15.8)(1.0)
Restructuring related costsRestructuring related costs(78.7)(4.1)Restructuring related costs(6.7)(78.7)
Share-based compensation expenseShare-based compensation expense(0.6)(0.4)Share-based compensation expense(0.5)(0.6)
Other special itemsOther special items(99.4)(99.5)Other special items(40.5)(99.4)
Adjusted cost of salesAdjusted cost of sales$1,900.6 $1,248.4 Adjusted cost of sales$1,705.1 $1,900.6 
Adjusted gross profit (a)
Adjusted gross profit (a)
$2,677.2 $1,482.8 
Adjusted gross profit (a)
$2,411.7 $2,677.2 
Adjusted gross margin (a)
Adjusted gross margin (a)
58 %54 %
Adjusted gross margin (a)
59 %58 %
____________
(a)U.S. GAAP gross profit is calculated as total revenues less U.S. GAAP cost of sales. U.S. GAAP gross margin is calculated as U.S. GAAP gross profit divided by total revenues. Adjusted gross profit is calculated as total revenues less adjusted cost of sales. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues.
Operating Expenses
Research & Development Expense
R&D expense for the three months ended June 30, 20212022 was $147.7$162.6 million, compared to $156.3$147.7 million for the comparable prior year period, a decreasean increase of $8.6$14.9 million. This decreaseincrease was primarily due to higher expenses in the comparable prior year period related to licensing arrangementscosts for products in development, partially offset by increased costs associated with the Upjohn Business in the current year period.under development.
Selling, General & Administrative Expense
SG&A expense for the three months ended June 30, 2021current quarter was $1.20 billion,$981.1 million, compared to $719.4 million$1.20 billion for the comparable prior year period, an increasea decrease of $485.4$223.7 million. The increasedecrease was primarily due to lower restructuring costs of approximately $162.3 million related to the Upjohn Business of $421.3 million and an increase of approximately $146.2 million for restructuring costs due to the implementation of the 2020 restructuring program. Partially offsetting these increases were lower acquisition related costsprogram and the impact of approximately $74.2 million and lower selling and promotional expenses, including through our active management related to synergies and certain lower expenses as a result of COVID-19.synergies.
Litigation Settlements and Other Contingencies, Net
The following table includes the losses/(gains)losses recognized in litigation settlements and other contingencies, net during the three months ended June 30, 2022 and 2021, and June 30, 2020:respectively:
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Three Months EndedThree Months Ended
June 30,June 30,
(In millions)(In millions)20212020(In millions)20222021
Respiratory delivery platform contingent consideration adjustment$22.9 $12.1 
Contingent consideration adjustment (primarily related to respiratory delivery platform)Contingent consideration adjustment (primarily related to respiratory delivery platform)$1.3 $22.9 
Litigation settlements, netLitigation settlements, net0.1 3.7 Litigation settlements, net9.6 0.1 
Total litigation settlements and other contingencies, netTotal litigation settlements and other contingencies, net$23.0 $15.8 Total litigation settlements and other contingencies, net$10.9 $23.0 
Interest Expense
Interest expense for the three months ended June 30, 20212022 totaled $167.1$145.9 million, compared to $116.2 million for the three months ended June 30, 2020, an increase of $50.9 million. The increase is due to the interest expense related to the additional debt assumed in the Combination of approximately $68.2 million, partially offset by amortization of debt premium of $17.3 million and by the impact of debt repayments in 2021.
Other Expense (Income), Net
Other expense, net was $4.2$167.1 million for the three months ended June 30, 2021, compareda decrease of $21.2 million. The decrease is primarily due to other income, netthe impact of $2.0 million for the comparable prior year period. debt repayments.
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Other Expense, Net
Other expense, (income), net includes losses from equity affiliates, foreign exchange gains and losses, expense (income) related to post-employment benefit plans and interest and dividend income. Other expense, (income), net was comprised of the following for the three months ended June 30, 2021 and 2020, respectively:2022 totaled $13.5 million, compared to $4.2 million for the three months ended June 30, 2021. The increase was primarily driven by lower costs associated with post-employment benefit plans in the prior year period.
Three Months Ended
June 30,
(In millions)20212020
Losses from equity affiliates, primarily clean energy investments$16.7 $17.2 
Foreign exchange losses, net8.8 3.8 
Other gains, net(21.3)(23.0)
Other expense (income), net$4.2 $(2.0)

Income Tax Provision
For the three months ended June 30, 2021,2022, the Company recognized an income tax provision of $60.1$75.4 million, compared to an income tax benefit of $19.4$60.1 million for the comparable prior year period, an increase of $79.5$15.3 million. The increase in the current year provision was due to the changing mix of income earned in jurisdictions with differing rates. The income tax provision for the three months ended June 30, 2021 was negatively impacted by the tax rates applied to the reversal of intercompany profit in inventory reserve which was recorded on the opening balance sheet as part of the Combination. This reserve eliminates the profit in inventory related to intercompany transactions and changes to this reserve occur as products are sold to third parties. Also impacting the current year income tax provision was the changing mix of income earned in jurisdictions with differing tax rates.

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Six Months Ended June 30, 20212022 Compared to Six Months Ended June 30, 20202021
Six Months EndedSix Months Ended
June 30,June 30,
(In millions, except %s)(In millions, except %s)20212020% Change
2021 Currency Impact (1)
2021 Constant Currency Revenues
Constant Currency % Change (2)
(In millions, except %s)20222021% Change
2022 Currency Impact (1)
2022 Constant Currency Revenues
Constant Currency % Change (2)
Net salesNet salesNet sales
Developed MarketsDeveloped Markets$5,212.0 $3,969.1 31 %$(209.1)$5,002.9 26 %Developed Markets$4,955.2 $5,212.0 (5)%$270.5 $5,225.8 — %
Greater ChinaGreater China1,142.2 37.8 nm(0.3)1,141.9 nmGreater China1,121.4 1,142.2 (2)%(2.7)1,118.7 (2)%
JANZJANZ982.9 523.4 88 %(36.9)946.0 81 %JANZ850.9 982.9 (13)%102.7 953.5 (3)%
Emerging MarketsEmerging Markets1,624.7 753.8 116 %(24.6)1,600.1 112 %Emerging Markets1,356.1 1,624.7 (17)%105.5 1,461.6 (10)%
Total net salesTotal net sales$8,961.8 $5,284.1 70 %$(270.9)$8,690.9 64 %Total net sales$8,283.6 $8,961.8 (8)%$476.0 $8,759.6 (2)%
Other revenues (3)
Other revenues (3)
46.3 66.3 (30)%(1.2)45.1 (32)%
Other revenues (3)
24.9 46.3 (46)%1.3 26.2 (43)%
Consolidated total revenues (4)
Consolidated total revenues (4)
$9,008.1 $5,350.4 68 %$(272.1)$8,736.0 63 %
Consolidated total revenues (4)
$8,308.5 $9,008.1 (8)%$477.3 $8,785.8 (2)%
____________
(1)Currency impact is shown as unfavorable (favorable).
(2)The constant currency percentage change is derived by translating net sales or revenues for the current period at prior year comparative period exchange rates, and in doing so shows the percentage change from 20212022 constant currency net sales or revenues to the corresponding amount in the prior year.
(3)For the six months ended June 30, 2021,2022, other revenues in Developed Markets, JANZ, and Emerging Markets were approximately $34.5$11.1 million, $1.0$0.9 million, and $10.8$12.9 million, respectively.
(4)Amounts exclude intersegment revenue thatwhich eliminates on a consolidated basis.
Total Revenues
For the six months ended June 30, 2021,2022, Viatris reported total revenues of $9.01$8.31 billion, compared to $5.35$9.01 billion for the comparable prior year period, representing an increasea decrease of $3.66 billion,$699.6 million, or 68%8%. Total revenues include both net sales and other revenues from third parties. Net sales for the six months ended June 30, 20212022 were $8.96$8.28 billion, compared to $5.28$8.96 billion for the comparable prior year period, representing an increasea decrease of $3.68 billion,$678.2 million, or 70%8%. Other revenues for the current yearsix months ended June 30, 2022 were $46.3$24.9 million, compared to $66.3$46.3 million for the comparable prior year period.
The increasedecrease in total revenues and net sales was primarily driven by net sales totaling $3.35 billion from the Upjohn Business in the current year and approximately $397.0 million of new product sales, partially offset by a decrease of approximately $340.7 million in net sales from existing products as a result of lower pricing, and to a lesser extent, lower volumes. New product sales include new products launched in 2021 and the carryoverunfavorable impact of new products, including business development, launched since July 1, 2020. The Company’s net sales were favorably impacted by the effect of foreign currency translation of approximately $476.0 million, or 5%, primarily reflecting changes in the U.S. Dollar as compared to the currencies of subsidiaries in countries within the EU and in Australia and India. The net favorable impact of foreign currency translation on net sales was approximately $270.9 million, or 5%.Japan. On a constant currency basis, the increasedecrease in net sales was approximately $3.41 billion,$202.2 million, or 65%2% for the six months ended June 30, 2021. We estimate that the COVID-19 pandemic positively impacted our2022. This decrease was due to competition on certain key U.S. products representing a decline of approximately $140 million and approximately $267 million as a result of other base business erosion. The decrease in net sales during the six months ended June 30, 2021from existing products was partially offset by approximately 1% as compared to$204.6 million of new product sales. New product sales include new products launched in 2022 and the prior year period.carryover impact of new products, including business development, launched within the last twelve months.
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, seasonality, and the amount, if any, of additional competition in the market. Our top ten products in terms of net sales, in the aggregate, represented approximately 34% and 24% for the six months ended June 30, 20212022 and 2020, respectively, with the year-over-year increase a result of the Combination. This percentage may fluctuate based upon the timing of new product launches, seasonality and the timing of changes in competition.2021.
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Net sales are derived from our four reporting segments: Developed Markets, Greater China, JANZ, and Emerging Markets.
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Developed Markets Segment
Net sales from Developed Markets increaseddecreased by $1.24 billion$256.8 million or 31%5% during the six months ended June 30, 20212022 when compared to the prior year period. This decrease was due primarily to the unfavorable impact of foreign currency translation of approximately $270.5 million, or 5%. Constant currency net sales increased by approximately $13.7 million, or less than 1% when compared to the prior year period. Net sales within North America totaled approximately $2.40$2.22 billion and net sales within Europe totaled approximately $2.81$2.74 billion. ThisThe increase was due primarily to net sales from the Upjohn Business in the current year of $1.05 billion,driven by new product sales, including the portfolio of thrombosis products in Europe acquired from AspenCyclosporine Ophthalmic Emulsion, Insulin Glargine and Semglee® in the fourth quarter of 2020,U.S., and higher volumes related to customer purchasing patternsof existing products in North America for the EpiPen® Auto-Injector, Yupelri, and biosimilar products. This increase wasEurope. These increases were partially offset by lower pricing and volumes on net sales of certain existing North Americankey products within the U.S., including Wixela, Xulane, Perforomist,Miacalcin® and Levothyroxine Sodium, due to additional competition. Lower volumes were also due to the impact of product divestitures, including certain North American OTC products during the current quarter and other products during 2020Perforomist®, as a result of the Combination. Sales of existing products in Europe were negatively impacted by lower pricing and lower volumes as a result of a decline in certain tender sales. The favorable impact of foreign currency translation on current period net sales, primarily in Europe, was approximately $209.1 million, or 5%. Constant currency net sales increased by approximately $1.03 billion, or 26% when compared to the prior year period.additional competition.

Greater China Segment
Net sales from Greater China increaseddecreased by $1.10 billion$20.8 million or 2% for the six months ended June 30, 20212022 when compared to the prior year period. This increasedecrease was the result of net sales from the Upjohn Business in the current year of $1.13 billion. This increase was partially offset by lower net sales of existing products, driven by lower volumes, whichvolumes. Volumes on net sales of existing products were negatively impacted by competitive and other market conditions, including VBP.conditions. The favorable impact of foreign currency translation was approximately $0.3$2.7 million, or less than 1%. Constant currency net sales increaseddecreased by approximately $1.10 billion$23.5 million or 2% when compared to the prior year.
JANZ Segment
Net sales from JANZ increaseddecreased by $459.5$132.0 million or 88%13% for the six months ended June 30, 2021 when compared to the prior year. This increase was the result of net sales from the Upjohn Business in the current year of $381.5 million and higher net sales of existing products driven by higher volumes in Japan primarily driven by the impact of the termination of the collaboration arrangement with Pfizer in the prior year, Amitiza, Lipacreon, and the EpiPen® Auto-Injector. These increases were partially offset by lower pricing and volumes in Australia driven by government price reductions and product competition. Foreign currency translation had a favorable impact of approximately $36.9 million, or 7%. Constant currency net sales increased by approximately $422.6 million, or 81%2022 when compared to the prior year period. This decrease was primarily the result of the unfavorable impact of foreign currency translation of approximately $102.7 million, or 10%. Constant currency net sales decreased by approximately $29.3 million, or 3% when compared to the prior year period. The decrease was primarily due to lower net sales of existing products mainly driven by lower pricing in Japan as a result of government price reductions and additional competition, and lower volumes on net sales of existing products in Australia. These decreases were partially offset by higher volumes on net sales of existing products in Japan, including for Celebrex®.
Emerging Markets Segment
Net sales from Emerging Markets increaseddecreased by $870.9$268.6 million or 116%17% for the six months ended June 30, 20212022 when compared to the prior year period. This increasedecrease was the resultmainly driven by lower volumes of net sales from the Upjohn Business in the current year of $783.3 million and COVID-19 related product salesproducts in India, primarily related to remdesivir and ambisome.ambisome, and lower sales of ARV products as a result of competitive market conditions. The decrease was further driven by the unfavorable impact of foreign currency translation. These increasesdecreases were partially offset by lower volumes and pricing of antiretroviral drugs as a result of the timing of orders across multiple markets, and lowerhigher volumes in other markets.certain markets in Asia. The favorableunfavorable impact of foreign currency translation was $24.6$105.5 million or 3%7%. Constant currency net sales increaseddecreased by approximately $846.3$163.1 million, or 112%10%.
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Cost of Sales and Gross Profit
Cost of sales increaseddecreased from $3.42 billion for the six months ended June 30, 2020 to $6.55 billion for the six months ended June 30, 2021.2021 to $4.83 billion for the six months ended June 30, 2022. Cost of sales was primarily impacted by purchase accounting related amortization of the fair value of step-up of acquired intangible assetsinventory of $953.7 million in the comparable prior year period, lower restructuring costs in the current period related to the 2020 restructuring program versus the comparable prior year period, and lower costs associated with other special items, which are described further in the section titled Use of Non-GAAP Financial Measures.
Gross profit for the six months ended June 30, 2022 was $3.47 billion and gross margins were 42%. For the six months ended June 30, 2021, gross profit was $2.46 billion and gross margins were 27%. ForThis change is primarily related to the six months ended June 30, 2020, gross profit was $1.93 billion and gross margins were 36%. Costdecrease in cost of sales from the Upjohn Business, including the impact of amortization expense, was $2.47 billion for the six months ended June 30, 2021. This includes increased amortization expense of $1.56 billion primarily for purchase accounting related amortization of intangible assets and the step-up of acquired inventory. Gross profit from net sales of existing products was impacted equally by lower volumes and lower pricing.sales. Adjusted gross margins were 59% for the six months ended June 30, 2021,2022, essentially flat when compared to 54% for the six months ended June 30, 2020, with the year-over-year increase driven by the impact2021.
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A reconciliation between cost of sales, as reported under U.S. GAAP, and adjusted cost of sales and adjusted gross margin for the six months ended June 30, 20212022 compared to the six months ended June 30, 20202021 is as follows:
Six Months EndedSix Months Ended
June 30,June 30,
(In millions, except %s)(In millions, except %s)20212020(In millions, except %s)20222021
U.S. GAAP cost of salesU.S. GAAP cost of sales$6,553.1 $3,418.6 U.S. GAAP cost of sales$4,834.0 $6,553.1 
Deduct:Deduct:Deduct:
Purchase accounting related amortizationPurchase accounting related amortization(2,424.8)(704.0)Purchase accounting related amortization(1,303.7)(2,424.8)
Acquisition related itemsAcquisition related items(3.5)(2.1)Acquisition related items(24.8)(3.5)
Restructuring related costsRestructuring related costs(246.5)(8.9)Restructuring related costs(19.8)(246.5)
Share-based compensation expenseShare-based compensation expense(1.2)(0.7)Share-based compensation expense(0.8)(1.2)
Other special itemsOther special items(186.1)(215.7)Other special items(81.5)(186.1)
Adjusted cost of salesAdjusted cost of sales$3,691.0 $2,487.2 Adjusted cost of sales$3,403.4 $3,691.0 
Adjusted gross profit (a)
Adjusted gross profit (a)
$5,317.1 $2,863.2 
Adjusted gross profit (a)
$4,905.1 $5,317.1 
Adjusted gross margin (a)
Adjusted gross margin (a)
59 %54 %
Adjusted gross margin (a)
59 %59 %
____________
(a)U.S. GAAP gross profit is calculated as total revenues less U.S. GAAP cost of sales. U.S. GAAP gross margin is calculated as U.S. GAAP gross profit divided by total revenues. Adjusted gross profit is calculated as total revenues less adjusted cost of sales. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues.
Operating Expenses
Research & Development Expense
R&D expense for the six months ended June 30, 20212022 was $331.8$304.9 million, compared to $270.5$331.8 million for the comparable prior year period, an increasea decrease of $61.3$26.9 million. This increasedecrease was primarily due to costs associated with the Upjohn Business of $65.7 million and increasedlower costs for inventory validation batches for certain products under development. These increases were partially offset by lower expenses indevelopment and the current year period related to licensing arrangements for products in development.
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synergies.
Selling, General & Administrative Expense
SG&A expense for the six months ended June 30, 20212022 was $2.39$1.90 billion, compared to $1.32$2.39 billion for the comparable prior year period, an increasea decrease of $1.07 billion.$494.9 million. The increasedecrease was primarily due to lower restructuring costs of approximately $299.8 million related to the Upjohn Business of $857.7 million and an increase of approximately $283.7 million for restructuring costs due to the implementation of the 2020 restructuring program. Partially offsetting these increases were lower acquisition related costsprogram and the impact of approximately $39.2 million and lower selling and promotional expenses, including through our active management related to synergies and certain lower expenses as a result of COVID-19.synergies.
Litigation Settlements and Other Contingencies, Net
The following table includes the losses/(gains)losses recognized in litigation settlements and other contingencies, net during the six months ended June 30, 20212022 and June 30, 2020:2021:
Six Months EndedSix Months Ended
June 30,June 30,
(In millions)(In millions)20212020(In millions)20222021
Respiratory delivery platform contingent consideration adjustment$32.0 $18.7 
Contingent consideration adjustment (primarily related to respiratory delivery platform)Contingent consideration adjustment (primarily related to respiratory delivery platform)$13.6 $32.0 
Litigation settlements, netLitigation settlements, net13.9 (1.1)Litigation settlements, net3.5 13.9 
Total litigation settlements and other contingencies, netTotal litigation settlements and other contingencies, net$45.9 $17.6 Total litigation settlements and other contingencies, net$17.1 $45.9 
Interest Expense
Interest expense for the six months ended June 30, 20212022 totaled $336.1$292.1 million, compared to $236.1 million for the six months ended June 30, 2020, an increase of $100.0 million. The increase is due to the interest expense related to the additional debt assumed in the Combination of approximately $143.8 million, partially offset by amortization of debt premium of $34.5 million and by the impact of debt repayments in 2021.
Other Expense (Income), Net
Other expense, net was $10.3$336.1 million for the six months ended June 30, 2021, compareda decrease of $44.0 million. The decrease is primarily due to $32.1 million for the comparable prior year period. impact of debt repayments.
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Other Expense, Net
Other expense, net includes losses from equity affiliates, foreign exchange gains and losses, expense (income) related to post-employment benefit plans and interest and dividend income. Other expense, net was comprised of the following$47.2 million for the six months ended June 30, 2021 and 2020, respectively:2022, compared to $10.3 million for the comparable prior year period. The increase was primarily driven by higher foreign exchange costs. The increase was partially offset by lower losses from clean energy investments.
Six Months Ended
June 30,
(In millions)20212020
Losses from equity affiliates, primarily clean energy investments$34.6 $34.5 
Foreign exchange losses, net8.6 17.4 
Other gains, net(32.9)(19.8)
Other expense, net$10.3 $32.1 

Income Tax Provision (Benefit)
For the six months ended June 30, 2021,2022, the Company recognized an income tax provision of $656.4$203.7 million, compared to an income tax benefit of $9.5$656.4 million for the comparable prior year period, an increasea decrease of $665.9$452.7 million. The income tax provision for the six months ended June 30, 2021 was negatively impacted by the tax rates applied to the reversal of intercompany profit in inventory reserve which was recorded on the opening balance sheet as part of the Combination. This reserve eliminates the profit in inventory related to intercompany transactions and changes to this reserve occur as products are sold to third parties. During the six months ended June 30, 2020, the Company recognized a benefit as a result of changes in the assessment of the realizability of deferred tax assets. Also impacting the current year income tax expense was the changing mix of income earned in jurisdictions with differing tax rates.


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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 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. Primarily due to acquisitions and other significant events which may impact comparability of our periodic operating results, 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. The Company’s use of such non-GAAP measures is governed by an adjusted reporting policy maintained by the Company and such non-GAAP measures are reviewed in detail with the Audit Committee of the Board of Directors.
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 related amortization, which are described in greater detail below.
Adjusted Net Earnings
Adjusted net 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 and other significant events, 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. Management believes that adjusted net earnings is an important internal financial metric related to the ongoing operating performance of the Company, and is therefore useful to investors and that their understanding of our performance is enhanced by this measure. Actual internal and forecasted operating results and annual budgets used by management include adjusted net earnings.
EBITDA and Adjusted EBITDA
EBITDA and adjusted EBITDA are non-GAAP financial measures that the Company believes are appropriate to provide additional information to investors to demonstrate the Company’s ability to comply with financial debt covenants and assess the Company’s ability to incur additional indebtedness. The Company also believes that adjusted EBITDA better focuses management on the Company’s underlying operational results and true business performance and, is used, in part, for management’s incentive compensation. We calculate “EBITDA”EBITDA as U.S. GAAP net earnings (loss) adjusted for net contribution attributable to equity method investments, income tax provision (benefit), interest expense and depreciation and amortization. EBITDA is further adjusted for share-based compensation expense, litigation settlements and other contingencies, net, and restructuring, acquisition related and other special items to determine “adjusted EBITDA”.adjusted EBITDA. These adjustments are generally permitted under our credit agreement in calculating Adjustedadjusted EBITDA for determining compliance with our debt covenants.
The significant items excluded from adjusted cost of sales, adjusted net earnings, and adjusted EBITDA include:
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Purchase Accounting Amortization and Other Related Items
The ongoing impact of certain amounts recorded in connection with acquisitions of both businesses and assets is excluded from adjusted cost of sales, adjusted net earnings, and adjusted EBITDA. These amounts include the amortization of intangible assets, inventory step-up, property, plant and equipment step-up, and intangible asset impairment charges, including for in-process research and development. For the acquisition of businesses accounted for under the provisions of ASC 805, Business Combinations, these purchase accounting impacts are excluded regardless of the financing method used for the acquisitions, including the use of cash, long-term debt, the issuance of common stock, contingent consideration or any combination thereof.
Upfront and Milestone-Related R&D Expenses
TheseBeginning in 2022, upfront and milestone-related R&D expenses related to collaboration and paymentslicensing arrangements are no longer excluded from adjusted net earnings and adjusted EBITDA. This change had no impact on the three and six months ended June 30, 2022. For all prior periods presented, these expenses and payments were excluded from adjusted net earnings and adjusted EBITDA. Prior period adjusted net earnings and adjusted EBITDA have not been recast to reflect this change in policy because they generally occur at irregular intervalsthe excluded amount was income of approximately $6.3 million and are not indicative of$5.8 million for the Company’s ongoing operations.three and six months ended June 30, 2021, respectively, and is considered immaterial.
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 net earnings and adjusted EBITDA 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 their exclusion is helpful to understanding the underlying, ongoing operational performance of the business.
Share-based Compensation Expense
Share-based compensation expense is excluded from adjusted net earnings and adjusted EBITDA. Our share-based compensation programs have become increasingly weighted toward performance-based compensation, which leads to variability and to a lack of predictability as to the occurrence and/or timing of amounts incurred. As such, management believes the exclusion of such amounts on an ongoing basis is helpful to understanding the underlying 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 net earnings and adjusted EBITDA, as applicable. These amounts include items such as:
Costs related to formal restructuring programs and actions, including costs associated with facilities to be closed or divested, employee separation costs, impairment charges, accelerated depreciation, incremental manufacturing variances, equipment relocation costs, decommissioning 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, certain financing related costs, certain reimbursements related to the Company’s obligation to reimburse Pfizer for certain financing and transaction related costs under the Business Combination Agreement and Separation and Distribution Agreement, certain other TSA related exit 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 the Code; only included in adjusted net earnings is the net tax effect of the entity’s activities;
Other costs, incurred from time to time, related to certain special events or activities that lead to gains or losses, including, but not limited to, incremental manufacturing variances, asset write-downs, or liability adjustments;
Certain costs to further develop and optimize our global enterprise resource planning systems, operations and supply chain; and
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The impact of changes related to uncertain tax positions and certain impacts related to the Combination are excluded from adjusted net earnings. In addition, tax adjustments to adjusted earnings are recorded to present items on an after-tax basis consistent with the presentation of adjusted net earnings.
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
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excludes these amounts from adjusted net earnings and adjusted EBITDA 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 Note 1817 Litigation included in Part I, Item 1 of this Form 10-Q are generally excluded from adjusted net earnings and adjusted EBITDA. Normal, ongoing defense costs of the Company made in the normal course of our business are not excluded.
Reconciliation of U.S. GAAP Net Earnings (Loss) Earnings to Adjusted Net Earnings
A reconciliation between net earnings (loss) earnings as reported under U.S. GAAP, and adjusted net earnings for the periods shown follows:
Three Months Ended June 30,Six Months Ended June 30,Three Months Ended June 30,Six Months Ended June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
U.S. GAAP net (loss) earnings$(279.2)$39.4 $(1,316.8)$60.2 
U.S. GAAP net earnings (loss)U.S. GAAP net earnings (loss)$313.9 $(279.2)$713.1 $(1,316.8)
Purchase accounting related amortization (primarily included in cost of sales) (a)
Purchase accounting related amortization (primarily included in cost of sales) (a)
1,169.8 351.8 2,424.8 704.0 
Purchase accounting related amortization (primarily included in cost of sales) (a)
644.9 1,169.8 1,303.8 2,424.8 
Litigation settlements and other contingencies, netLitigation settlements and other contingencies, net23.0 15.8 45.9 17.6 Litigation settlements and other contingencies, net10.9 23.0 17.1 45.9 
Interest expense (primarily amortization of premiums and discounts on long term debt)Interest expense (primarily amortization of premiums and discounts on long term debt)(13.4)5.5 (26.7)11.3 Interest expense (primarily amortization of premiums and discounts on long term debt)(13.1)(13.4)(26.8)(26.7)
Clean energy investments pre-tax lossClean energy investments pre-tax loss16.7 17.2 34.6 34.5 Clean energy investments pre-tax loss0.1 16.7 — 34.6 
Acquisition related costs (primarily included in SG&A) (b)(a)
Acquisition related costs (primarily included in SG&A) (b)(a)
48.4 122.7 108.2 145.9 
Acquisition related costs (primarily included in SG&A) (b)(a)
122.4 48.4 207.1 108.2 
Restructuring related costs (c)(b)
Restructuring related costs (c)(b)
254.7 23.6 570.1 32.5 
Restructuring related costs (c)(b)
10.2 254.7 27.0 570.1 
Share-based compensation expenseShare-based compensation expense31.0 15.3 63.7 34.7 Share-based compensation expense29.4 31.0 57.7 63.7 
Other special items included in:Other special items included in:Other special items included in:
Cost of sales (d)(c)
Cost of sales (d)(c)
99.4 99.5 186.1 215.7 
Cost of sales (d)(c)
40.5 99.4 81.5 186.1 
Research and development expense (e)
Research and development expense (e)
(6.3)40.4 8.4 42.1 
Research and development expense (e)
0.6 (6.3)0.9 8.4 
Selling, general and administrative expenseSelling, general and administrative expense10.2 9.1 29.5 5.4 Selling, general and administrative expense17.0 10.2 24.4 29.5 
Other expense, netOther expense, net— (16.1)— (16.4)Other expense, net(0.4)— (1.9)— 
Tax effect of the above items and other income tax related items (f)(d)
Tax effect of the above items and other income tax related items (f)(d)
(173.7)(149.9)169.2 (246.0)
Tax effect of the above items and other income tax related items (f)(d)
(111.1)(173.7)(213.3)169.2 
Adjusted net earningsAdjusted net earnings$1,180.6 $574.3 $2,297.0 $1,041.5 Adjusted net earnings$1,065.3 $1,180.6 $2,190.6 $2,297.0 
Significant items include the following:
(a)For the three and six months ended June 30, 2021 includes amortization of the purchase accounting inventory fair value adjustment related to the Combination totaling approximately $477.3 million and $953.7 million, respectively.
(b)Acquisition related costs consist primarily of transaction costs including legal and consulting fees and integration activities. Refer to SG&A discussion within the section “Three Months Ended June 30, 2021 Compared to Three Months Ended June 30, 2020” and “Six Months Ended June 30, 2021 Compared to Six Months Ended June 30, 2020”.
(c)(b)For the three months ended June 30, 2021 charges of approximately $78.7 million are included in cost of sales, approximately $10.2 million are included in R&D, and approximately $165.8 million are included in SG&A. For the six months ended June 30, 20212022, charges ofinclude approximately $246.5$6.7 million are includedand $19.8 million, respectively, in cost of sales approximately $16.6 million are included in R&D, and approximately $307.0$3.5 million are includedand $7.2 million, respectively, in SG&A. Refer to Note 1514 Restructuring included in Part I, Item 1 of this Form 10-Q for additional information.
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(d)(c)Costs incurred during the three months and six months ended June 30, 2021 include incremental manufacturing variances and site remediation activities as a result of the activities at the Company’s Morgantown plant of approximately $44.1 million and $89.1 million, respectively. Costs incurred duringFor the three and six months ended June 30, 2020 primarily relate to2022, charges include incremental manufacturing variances and site remediation activities as a result ofat plants in the activities at the Company’s Morgantown plant2020 restructuring program of approximately $63.0$16.5 million and $121.8$47.8 million, respectively. In addition, the three and six months ended June 30, 2020 includes incremental manufacturing variances incurred as a result of the COVID-19 pandemic of approximately $15.0 million and $22.0 million, respectively. Also, the six months ended June 30, 2020 includes $25.0 million related to a special bonus for plant employees as a result of the COVID-19 pandemic.
(e)Adjustments primarily relate to non-refundable payments related to development agreements.
(f)(d)Adjusted for changes for uncertain tax positions and for certain impacts of the Combination.
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Reconciliation of U.S. GAAP Net Earnings (Loss) Earnings to EBITDA and Adjusted EBITDA
Below is a reconciliation of U.S. GAAP net earnings (loss) earnings to EBITDA and adjusted EBITDA for the three and six months ended June 30, 20212022 compared to the prior year period:
Three Months Ended June 30,Six Months Ended June 30,Three Months Ended June 30,Six Months Ended June 30,
(In millions)(In millions)2021202020212020(In millions)2022202120222021
U.S. GAAP net (loss) earnings$(279.2)$39.4 $(1,316.8)$60.2 
U.S. GAAP net earnings (loss)U.S. GAAP net earnings (loss)$313.9 $(279.2)$713.1 $(1,316.8)
Add adjustments:Add adjustments:Add adjustments:
Net contribution attributable to equity method investmentsNet contribution attributable to equity method investments16.7 17.2 34.6 34.5 Net contribution attributable to equity method investments0.1 16.7 — 34.6 
Income tax provision (benefit)60.1 (19.4)656.4 (9.5)
Income tax provisionIncome tax provision75.4 60.1 203.7 656.4 
Interest expense (a)
Interest expense (a)
167.1 116.2 336.1 236.1 
Interest expense (a)
145.9 167.1 292.1 336.1 
Depreciation and amortization (b)
Depreciation and amortization (b)
1,317.1 415.7 2,739.6 830.7 
Depreciation and amortization (b)
722.3 1,317.1 1,458.3 2,739.6 
EBITDAEBITDA$1,281.8 $569.1 $2,449.9 $1,152.0 EBITDA$1,257.6 $1,281.8 $2,667.2 $2,449.9 
Add adjustments:Add adjustments:Add adjustments:
Share-based compensation expenseShare-based compensation expense31.0 15.3 63.7 34.7 Share-based compensation expense29.4 31.0 57.7 63.7 
Litigation settlements and other contingencies, netLitigation settlements and other contingencies, net23.0 15.8 45.9 17.6 Litigation settlements and other contingencies, net10.9 23.0 17.1 45.9 
Restructuring, acquisition related and other special items (c)
Restructuring, acquisition related and other special items (c)
339.6 278.4 752.5 425.0 
Restructuring, acquisition related and other special items (c)
184.2 339.6 326.4 752.5 
Adjusted EBITDAAdjusted EBITDA$1,675.4 $878.6 $3,312.0 $1,629.3 Adjusted EBITDA$1,482.1 $1,675.4 $3,068.4 $3,312.0 
(a)    Includes amortization of premiums and discounts on long-term debt.
(b)    Includes purchase accounting related amortization.
(c)    See items detailed in the Reconciliation of U.S. GAAP Net Earnings (Loss) Earnings to Adjusted Net Earnings.
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Liquidity and Capital Resources
Our primary source of liquidity is net cash provided by operating activities, which was $1.41$1.94 billion for the six months ended June 30, 2021.2022. We believe that net cash provided by operating activities and available liquidity will continue to allow us to meet our needs for working capital, capital expenditures, interest and principal payments on debt obligations, and dividend payments. Nevertheless, our ability to satisfy our working capital requirements and debt service obligations, fund planned capital expenditures, or dividend payments, 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
Net cash provided by operating activities increased by $737.6$532.8 million to $1.41$1.94 billion for the six months ended June 30, 2021,2022, as compared to net cash provided by operating activities of $670.6 million$1.41 billion for the six months ended June 30, 2020.2021. Net cash provided by operating activities is derived from net earnings (loss) 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.
vtrs-20210630_g1.jpg
NetThe increase in net cash provided by operating activities was favorably impacted inprincipally due to lower payments for restructuring activities and other special items, and the current year period by higher operating earnings, after adjusting for non-cash items in both periods,impact of the combined company when compared to the prior year period. This increase was primarilysynergies, partially offset by the negative impact of the timing of income taxcash payments and collections on accounts receivable balances.collections.
Investing Activities
Net cash fromused in investing activities was $149.0 million for the six months ended June 30, 2022, as compared to net cash provided by investing activities of $219.5 million for the six months ended June 30, 2021, as compared toa net cash useddecrease of $368.5 million.
In 2022, significant items in investing activities of $220.1 millionincluded the following:
capital expenditures, primarily for equipment and facilities, totaling approximately $148.4 million. While there can be no assurance that current expectations will be realized, capital expenditures for the six months ended June 30, 2020, a net increase2022 calendar year are expected to be approximately $425 million to $575 million.
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vtrs-20210630_g2.jpg
In 2021, significant items in investing activities included the following:
cash received from acquisitions, net totaling approximately $277.0 million related to additional target cash balances received from Pfizer subsequent to the closing of the Combination;
proceeds from sale of assets of $83.4 million related to a group of OTC products in the U.S.; and
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capital expenditures, primarily for equipment and facilities, totaling approximately $138.8 million. While there can be no assurance that current expectations will be realized, capital expenditures for the 2021 calendar year are expected to be approximately $500 million to $650 million.million; and
payments for product rights and other, net totaling approximately $17.3 million, primarily related to the acquisition of intellectual property rights and marketing authorizations;
In 2020, significant items in investing activities included the following:
payments for product rights and other, net totaling approximately $76.4 million, primarily related to deferred non-contingent purchase payments for the acquisition of intellectual property rights and marketing authorizations in prior periods;
purchase of marketable securities and other investments of $90.2 million; and
capital expenditures, primarily for equipment and facilities, totaling approximately $87.9 million.authorizations.
Financing Activities
Net cash used in financing activities was $1.79 billion for the six months ended June 30, 2021,2022, as compared to $609.1 million$1.79 billion for the six months ended June 30, 2020, a net2021, an increase of $1.18 billion.$3.3 million.
In 2022, significant items in financing activities included the following:

long-term debt payments of approximately $1.79 billion consisting of the repayment of the 0.816% Euro Senior Notes due 2022 and the 1.125% Senior Notes due 2022;
vtrs-20210630_g3.jpglong-term debt borrowings of $795.4 million primarily consisting of Revolving Facility borrowings;
net repayments of short-term borrowings of $473.5 million; and
cash dividends paid of $290.6 million.
In 2021, significant items in financing activities included the following:
long-term debt payments of $2.25 billion consisting of the redemptionrepayment of the 3.150% Senior Notes due 2021;
long-term borrowings under the 2020 Revolving Facility of $900.0 million;
net short-term borrowings of $199.7 million;
cash dividends paid of $133.0 million;
deferred non-contingent payments for product rights totaling approximately $456.0 million primarily related to the acquisition of Aspen’s thrombosis product portfolio in Europe; and
milestone payments totaling approximately $28.6 million related to the respiratory delivery platform contingent consideration.
In 2020, significant items in financing activities included the following:
long-term debt payments of approximately $589.0 million consisting primarily of the redemption of $555.2 million principal amount of the 2020 Floating Rate Euro Notes; and
payments totaling $43.6 million of the $52.3 million in milestone payments related to the respiratory delivery platform contingent consideration. The remaining payments related to the respiratory delivery platform contingent consideration are included as a component of other operating assets and liabilities, net within net cash from operating activities.
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Capital Resources
Our cash and cash equivalents totaled $673.9$664.7 million at June 30, 2021,2022, and the majority of these funds are held by our non-U.S. subsidiaries. The Company anticipates having sufficient liquidity, including existing borrowing capacity under the 2021 Revolving Facility, Commercial Paper Program and the Receivables Facility and the Note Securitization Facility combined with cash to be generated from operations, to fund foreseeable cash needs without requiring the repatriation of non-U.S. cash.
In July 2021, Viatris entered into (i) the YEN Term Loan and (ii) the 2021 Revolving Facility with various syndicates of banks. The 2021 Revolving Facility amended and restated the 2020 Revolving Facility and proceeds from the 2021 Revolving Facility were used to repay outstanding obligations under the 2020 Revolving Facility. Proceeds from the YEN Term Loan and 2021 Revolving Facility were also used to repay the USD Term Loan in full and the USD Term Loan was terminated. The 2021 Revolving Facility and the YEN Term Loan have substantially identical terms to the 2020 Revolving Facility and USD Term Loan, respectively, with the following exceptions: 1) the maturity of both the YEN Term Loan and the 2021 Revolving Facility is July 2026, 2) the pricing was adjusted to reflect current market prices (which were generally more favorable) and 3) the maximum leverage ratio as of the end of any quarter was set at 4.25 to 1.00 for each quarter ending after June 30, 2021 through and including June 30, 2022, 4.0 to 1.00 for each quarter ending after June 30, 2022 through and including December 31, 2022 and 3.75 to 1.00 thereafter, except in circumstances as defined in the related credit agreement. The Company expects to designate the YEN Term Loan as a hedge of its investment in certain Yen-functional currency subsidiaries in order to manage foreign currency translation risk. Prior to July 2021, the maximum leverage ratio under the 2020 Revolving Facility was 4.25 to 1.00 for the first four full fiscal quarters following the close of the Combination.
The Company has access to $4.0 billion under the 2021 Revolving Facility which matures in July 2026. Up to $1.65 billion of the 2021 Revolving Facility may be used to support borrowings under our Commercial Paper Program. As of June 30, 2021,2022, the Company had $900$620.8 million outstanding under the 2020 Revolving Facility prior to entering into the 2021 Revolving Facility, which amendedCommercial Paper Program and restated the 2020 Revolving Facility as described above, and $600had borrowings outstanding of $795.0 million outstanding under the USD Term Loan, which was replaced by the YEN Term Loan as described above.Revolving Facility.
In addition to the 2021 Revolving Facility, MPI, a wholly owned subsidiary of the Company, has access to $400 million under the Receivables Facility. On April 22, 2022, the Company entered into an agreement to extend the expiration date of the Receivables Facility which expires into April 2022.22, 2025. As of June 30, 2021,2022, the Company had $400$198.7 million outstanding under the Receivables Facility.
In August 2020, the Company entered into the Note Securitization Facility for borrowings up to $200 million, which was amended on July 1, 2021 to extend the term to August 30, 2022. As of June 30, 2021,2022, the Company had $200borrowings of $200.0 million outstanding under the Note Securitization Facility.
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Under the terms of each of the Receivables Facility and Note Securitization Facility, certain of our accounts receivable secure the amounts borrowed and cannot be used to pay our other debts or liabilities. The amount that we may borrow at a given point in time is determined based on the amount of qualifying accounts receivable that are present at such point in time. Borrowings outstanding under the Receivables Facility bear interest at a commercial paperthe applicable base rate plus 0.925%0.775% and under the Note Securitization Facility at athe relevant base rate per annum quoted from time to time by MUFG Bank, Ltd. plus 1.00% (0.85% after the amendment of the Note Securitization Facility on July 1, 2021)0.85% and are included as a component of short-term borrowings, while the accounts receivable securing these obligations remain as a component of accounts receivable, net, in our condensed consolidated balance sheets. In addition, the agreements governing the Receivables Facility and Note Securitization Facility contain various customary affirmative and negative covenants, and customary default and termination provisions.
We have entered into accounts receivable factoring agreements with financial institutions to sell certain of our non-U.S. accounts receivable. These transactions are accounted for as sales and result in a reduction in accounts receivable because the agreements transfer effective control over and risk related to the receivables over to the buyers. Our factoring agreements do not allow for recourse in the event of uncollectibility, and we do not retain any interest in the underlying accounts receivable once sold. We derecognized $112.9$41.9 million and $153.0$29.6 million of accounts receivable as of June 30, 20212022 and December 31, 20202021 under these factoring arrangements, respectively.
At June 30, 2021, our long-term debt, including the current portion, totaled $23.07 billion, as compared to $24.69 billion at December 31, 2020. Total long-term debt is calculated net of deferred financing fees which were $44.7 million and $49.2 million at June 30, 2021 and December 31, 2020, respectively.
For additional information regarding our debtdividends paid and debt agreementsdeclared, refer to Note 128 DebtEarnings (Loss) per Share in Part I, Item 1 of this Form 10-Q.
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On May 7, 2021, the Company’s Board of Directors declared an inaugural quarterly cash dividend of $0.11 per share on the Company’s issued and outstanding common stock. The first quarterly cash dividend was paid on June 16, 2021 to shareholders of record as of the close of business on May 24, 2021. On August 6, 2021, the Company’s Board of Directors declared its second quarterly cash dividend of $0.11 per share on the Company’s issued and outstanding common stock, which will be payable on September 16, 2021 to shareholders of record as of the close of business on August 24, 2021. The declaration and payment of future dividends to holders of the Company’s common stock will be at the discretion of the Board of Directors, and will depend upon factors, including but not limited to, the Company’s financial condition, earnings, capital requirements of its businesses, legal requirements, regulatory constraints, industry practice, and other factors that the Board of Directors deems relevant.
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. Also, 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. In addition, we plan to continue to explore various other ways to create, enhance or otherwise unlock the value of the Company’s unique global platform in order to create shareholder value.
Long-term Debt Maturity
MandatoryFor information regarding our debt agreements and mandatory minimum repayments remaining on the outstanding notional amount of long-term debt at June 30, 2021 was as follows for each2022, refer to Note 11 Debt in Part I, Item 1 of the periods ending December 31:
vtrs-20210630_g4.jpgthis Form 10-Q.
The Company’s YEN Term Loan Facility and 2021the Revolving Facility (and, prior to July 2021, the 2020 Revolving Facility and USD Term Loan) 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 Company is in compliance with its covenants at June 30, 20212022 and expects to remain in compliance for the next twelve months.
Supplemental Guarantor Financial Information
Subsequent toViatris Inc. is the issuer of the Registered Upjohn Notes, which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan Inc., Mylan II B.V. and Utah Acquisition Sub Inc.
Following the Combination, Utah Acquisition Sub Inc. is the issuer of the 3.150% SeniorUtah U.S. Dollar Notes, due 2021, 3.950% Senior Notes due 2026 and 5.250% Senior Notes due 2046 (collectively, the “Utah Senior Notes”), which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan Inc., Viatris Inc. and Mylan II B.V.
Mylan Inc. is the issuer of the 4.200% SeniorMylan Inc. U.S. Dollar Notes, due 2023, 4.550% Senior Notes due 2028, 5.400% Senior Notes due 2043 and 5.200% Senior Notes due 2048 (collectively, the “Mylan Inc. Senior Notes” and, together with the Utah Senior Notes, the “Senior Notes”), which are fully and unconditionally guaranteed on a senior unsecured basis by Mylan II B.V., Viatris Inc. and Utah Acquisition Sub Inc.

The respective obligations of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc., and Mylan II B.V. as guarantors of the applicable series of Senior U.S. Dollar Notes as applicable, are senior unsecured obligations of the applicable guarantor and rank pari passu in right of payment with all of such guarantor’s existing and future senior unsecured obligations that are not expressly subordinated to
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such guarantor’s guarantee of the applicable series of Senior U.S. Dollar Notes, rank senior in right of payment to any future obligations of such guarantor that are expressly subordinated to such guarantor’s guarantee of the applicable series
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of Senior U.S. Dollar Notes, and are effectively subordinated to such guarantor’s existing and future secured obligations to the extent of the value of the collateral securing such obligations. The respectiveSuch obligations of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc., and Mylan II B.V. as guarantors of the Senior Notes, as applicable, are structurally subordinated to all of the existing and future liabilities, including trade payables, of the existing and future subsidiaries of such guarantor that do not guarantee the applicable series of Senior U.S. Dollar Notes.
The guarantees by ViatrisMylan Inc., Mylan Inc. and Mylan II B.V. and Utah Acquisition Sub Inc. under the applicable series of the Utah Senior U.S. Dollar Notes will terminate under certain customary circumstances, each as described in the following customary circumstances:applicable indenture, including: (1) a sale or disposition of Mylan Inc.the applicable guarantor in a transaction that complies with the applicable indenture such that Mylan Inc.such guarantor ceases to be a subsidiary of Viatris Inc.;the issuer of the applicable series of Senior U.S. Dollar Notes; (2) legal defeasance or covenant defeasance each as described in the applicable indenture, or if Utah Acquisition Sub Inc.’sthe issuer’s obligations under the applicable indenture are discharged; ordischarged; (3) with respect to the Utah U.S. Dollar Notes, the earlier to occur of (i) with respect to the guarantee provided by Mylan Inc., (x) the release of their respective guaranteesUtah Acquisition Sub Inc.’s guarantee under all applicable Mylan Inc. debtDebt (as defined in the applicable indenture) and (ii)(y) Mylan Inc. no longer having any obligations in respect of any Mylan Inc. debt.Debt and (ii) with respect to the guarantee provided by Mylan II B.V., (x) the release of Mylan II B.V.’s guarantee under all applicable Triggering Indebtedness (as defined in the applicable indenture) and (y) the issuer and/or borrower of the applicable Triggering Indebtedness no longer having any obligations with respect to such Triggering Indebtedness; (4) with respect to the guarantees provided by Utah Acquisition Sub Inc. and Mylan II B.V. of the Mylan Inc. U.S. Dollar Notes, subject to certain exceptions set forth in the applicable indenture, such guarantor ceasing to be a guarantor or obligor in respect of any Triggering Indebtedness; and (5) with respect to the Registered Upjohn Notes, (a) upon the applicable guarantor no longer being an issuer or guarantor in respect of (i) Mylan Notes (as defined in the indenture governing the Registered Upjohn Notes) that have an aggregate principal amount in excess of $500.0 million or (ii) any Triggering Indebtedness; in each case, other than in respect of indebtedness or guarantees, as applicable, that are being concurrently released; or (b) upon receipt of the consent of holders of a majority of the aggregate principal amount of the outstanding notes of such series in accordance with the indenture governing the Registered Upjohn Notes.
The guarantee obligations of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc., and Mylan II B.V. under the Senior U.S. Dollar Notes are subject to certain limitations and terms similar to those applicable to other guarantees of similar instruments, including that (i) the guarantees are subject to fraudulent transfer and conveyance laws and (ii) each guarantee is limited in amount to an amount not to exceed the maximum amount that can be guaranteed by the applicable guarantor without rendering the guarantee, as it relates to such guarantor, voidable under applicable fraudulent transfer and conveyance laws or similar laws affecting the rights of creditors generally.

The following table presents unaudited summarized financial information of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc., and Mylan II B.V. on a combined basis as of and for the six months ended June 30, 20212022 and as of and for the year ended December 31, 2020.2021. All intercompany balances have been eliminated in consolidation. This unaudited combined summarized financial information is presented utilizing the equity method of accounting.
Combined Summarized Balance Sheet Information of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc. and Mylan II B.V.Combined Summarized Balance Sheet Information of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc. and Mylan II B.V.
(In millions)(In millions)June 30, 2021December 31, 2020(In millions)June 30, 2022December 31, 2021
ASSETSASSETSASSETS
Current assetsCurrent assets$244.6 $477.7 Current assets$328.9 $280.2 
Non-current assetsNon-current assets60,417.1 61,272.4 Non-current assets60,171.7 60,298.0 
LIABILITIES AND EQUITYLIABILITIES AND EQUITYLIABILITIES AND EQUITY
Current liabilitiesCurrent liabilities22,071.5 20,951.7 Current liabilities24,424.0 23,619.9 
Non-current liabilitiesNon-current liabilities17,383.3 17,844.2 Non-current liabilities16,271.1 16,465.6 
Combined Summarized Income Statement Information of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc. and Mylan II B.V.
(In millions)Six-Months Ended June 30, 2021Year Ended December 31, 2020
Revenues$— $— 
Gross Profit— — 
Loss from Operations(545.0)(929.6)
Net loss(1,316.8)(669.9)
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Combined Summarized Income Statement Information of Viatris Inc., Mylan Inc., Utah Acquisition Sub Inc. and Mylan II B.V.
(In millions)Six Months Ended June 30, 2022Year Ended December 31, 2021
Revenues$— $— 
Gross profit— — 
Loss from operations(483.9)(1,023.9)
Net earnings (loss)713.1 (1,269.1)
Other Commitments
The Company is involved in various disputes, governmental and/or regulatory inquiries, investigations and proceedings, tax proceedings and litigation matters, both in the U.S. and abroad, that arise from time to time, some of which could result in losses, including damages, fines and/or civil penalties, and/or criminal charges against the Company. These
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matters are often complex and have outcomes that are difficult to predict. We have approximately $455.6$570.3 million accrued for legal contingencies at June 30, 2021.2022. In July 2022, the accrual was reduced by $259.0 million as a result of the EpiPen® Auto-Injectorsettlement payment. Refer to Note 17 Litigation in Part I, Item 1 of this Form 10-Q for additional information.
While the Company believes that it has meritorious defenses with respect to the claims asserted against it and the assumed legal matters referenced above, and intends to vigorously defend its position, the process of resolving these matters is inherently uncertain and may develop over a long period of time, and so it is not possible to predict the ultimate resolution of any such matter. It is possible that an unfavorable resolution of any of the ongoing matters could have a material effect on the Company’s business, financial condition, results of operations, cash flows, ability to pay dividends and/or stock price.
In conjunction with the Combination, Viatris entered into a TSA with Pfizer pursuant to which each party will provide certain limited transition services to the other party generally for an initial period of 24 months from the closing date of the Combination. In addition to the monthly service fees under the TSA, Viatris has agreed to reimburse Pfizer for fifty percent of the costs, up to the first $380 million incurred, to establish and wind down the TSA services. Viatris will be required to fully reimburse Pfizer for total costs in excess of $380 million. During the three and six months ended June 30, 2021,2022, the Company has incurred approximately $10.0$9.5 million and $26.3$26.1 million, respectively, related to this provision of the TSA and approximately $79.4$109.6 million during the period beginning on the closing date of the Combination and ended June 30, 2021.2022.
Application of Critical Accounting Policies
There have been no changes to the Critical Accounting Policies disclosed in Viatris’ 20202021 Form 10-K. The following discussion supplements our Critical Accounting Policy for Acquisitions, Intangible Assets, Goodwill and Contingent Consideration as it relates to the interim and annual goodwill impairment test performed as of March 31, 2022 and April 1, 2021.2022, respectively.
The Company has performed both its interim and annual goodwill impairment test as of April 1, 2021tests on a quantitative basis for its five reporting units, North America, Europe, Emerging Markets, JANZ, and Greater China. Additionally, the net assets acquired as part of the Combination were included in the respective reporting units and in the annual impairment test for the first time. In estimating each reporting unit’s fair value, the Company performed an extensive valuation analysis, utilizing both income and market-based approaches. The determination of the fair value of the reporting units requires the Company to make significant estimates and assumptions that affect the reporting unit’s expected future cash flows. These estimates and assumptions, utilizing Level 3 inputs, primarily include, but are not limited to, market multiples, control premiums, the discount rate, terminal growth rates, operating income before depreciation and amortization, and capital expenditures forecasts.
As of March 31, 2022 and April 1, 2021,2022, the allocation of the Company’s total goodwill (prior to the reclassification of goodwill to assets held for sale) was as follows: North America $3.66$3.61 billion, Europe $5.15$4.95 billion, Emerging Markets $1.58$1.64 billion, JANZ $0.82$0.78 billion and Greater China $0.70$0.97 billion.
As of March 31, 2022 and April 1, 2021,2022, the Company determined that the fair value of the North America Emerging Markets and Greater China reporting units was substantially in excess of the respective unit’s carrying value.
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For the Europe reporting unit, the estimated fair value exceeded its carrying value by approximately $0.91 billion$797 million or 5.8%5.3% for both the interim and annual goodwill impairment test.tests. As it relates to the income approach for the Europe reporting unit at March 31, 2022 and April 1, 2021,2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately 3.0%0.5%. A terminal year value was calculated with a 0.9%negative 1.0% revenue growth rate applied. The discount rate utilized was 10.5%9.5% and the estimated tax rate was 19.0%15.3%. Under the market-based approach, we utilized an estimated range of market multiples of 7.5 to 8.58.0 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by 2.9%3.0% or an increase in discount rate by 1.5% would result in an impairment charge for the Europe reporting unit.

For the JANZ reporting unit, the estimated fair value exceeded its carrying value by approximately $0.23 billion$231 million or 7.0%7.4% for both the interim and annual goodwill impairment test.tests. As it relates to the income approach for the JANZ reporting unit at March 31, 2022 and April 1, 2021,2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately negative 1.5%4.8%. A terminal year value was calculated with a 0.7%assuming no revenue growth rate applied.growth. The discount rate utilized was 8.5%6.0% and the estimated tax rate was 30.5%30.4%. Under the market-based approach, we utilized an estimated market multiple of 6.0 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by 4.2%3.5% or an increase in discount rate by 2.0% would result in an impairment charge for the JANZ reporting unit.
For the Emerging Markets reporting unit, the estimated fair value exceeded its carrying value by approximately $816 million or 10.3% for both the interim and annual goodwill impairment tests. As it relates to the income approach for the Emerging Markets reporting unit at March 31, 2022 and April 1, 2022, the Company forecasted cash flows for the next 10 years. During the forecast period, the revenue compound annual growth rate was approximately 1.6%. A terminal year value was calculated with a 0.8% revenue growth rate applied. The discount rate utilized was 10.5% and the estimated tax rate was 18.4%. Under the market-based approach, we utilized an estimated market multiple of 7.5 times EBITDA plus a control premium of 15.0%. If all other assumptions are held constant, a reduction in the terminal value growth rate by approximately 8.5% or an increase in discount rate by 3.0% would result in an impairment charge for the Emerging Markets reporting unit.
Due to the inherent uncertainty involved in making these estimates, actual results could differ from those estimates. In addition, changes in underlying assumptions, especially as they relate to the key assumptions detailed, could have a significant impact on the fair value of the reporting units.
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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 Viatris’ 20202021 Form 10-K.

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 June 30, 2021.2022. 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 has not identified any changesthe following change in the Company’s internal control over financial reporting (“ICFR”) that occurred during the second quarter of 2021 that havehas materially affected, or areis reasonably likely to materially affect, the Company’s ICFR. During the quarter ended June 30, 2022, the Company continued to transition certain support services from Pfizer, as well as certain subsidiaries, to a new ERP system. The Company has modified and will continue to modify its internal controls relating to its business and financial processes throughout the transition period, which is expected through the end of calendar year 2022. 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 over financial reporting.changes in order to provide certification as of its fiscal year ending December 31, 2022 on the effectiveness of its ICFR.
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PART II — OTHER INFORMATION
ITEM 1.    LEGAL PROCEEDINGS
For information regarding legal proceedings, refer to Note 1817 Litigation, in the accompanying Notes to interim financial statements in this Form 10-Q.
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ITEM 1A.     RISK FACTORS
There have been no material changes in the Company’s risk factors from those disclosed in Viatris’ 20202021 Form 10-K.
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ITEM 6. EXHIBITS
Amended and Restated Revolving Credit Agreement, dated as of July 1, 2021, among Viatris, the guarantors from time to time party thereto, the lenders and issuing banks from time to time party thereto and Bank of America, N.A., as administrative agent, filed as Exhibit 10.1 to the Report on Form 8-K filed by Viatris Inc. with the SEC on July 1, 2021, and incorporated herein by reference.*
Term Loan Credit Agreement, dated as of July 1, 2021, among Viatris, the guarantors from time to time party thereto, the lenders from time to time party thereto and Mizuho Bank, Ltd., as administrative agent, filed as Exhibit 10.2 to the Report on Form 8-K filed by Viatris Inc. with the SEC on July 1, 2021, and incorporated herein by reference.*
List of Subsidiary Guarantorssubsidiary guarantors and Issuersissuers of Guaranteed Securities, filed by Viatris Inc. as Exhibit 22 to the Form 10-K for the year ended December 31, 2020 and incorporated herein by reference.guaranteed securities.
Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
101.INSInline XBRL Instance Document
101.SCHInline XBRL Taxonomy Extension Schema
101.CALInline XBRL Taxonomy Extension Calculation Linkbase
101.DEFInline XBRL Taxonomy Definition Linkbase
101.LABInline XBRL Taxonomy Extension Label Linkbase
101.PREInline XBRL Taxonomy Extension Presentation Linkbase
104Cover Page Interactive Data File - the cover page interactive data file does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document (included in Exhibit 101).
*Annexes, schedules and/or exhibits have been omitted pursuant to Item 601(a)(5) of Regulation S-K. Viatris agrees to furnish supplementally a copy of any omitted attachment to the SEC on a confidential basis upon request.

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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.
Viatris Inc.
By:/s/ MICHAEL GOETTLER
 Michael Goettler
 Chief Executive Officer
 (Principal Executive Officer)
August 9, 20218, 2022
/s/ SANJEEV NARULA
 Sanjeev Narula
 Chief Financial Officer
 (Principal Financial Officer)
August 9, 20218, 2022
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