ADMA Biologics (ADMA) 10-Q 5 Aug 20 2020 Q2 Quarterly report Financial data

Cover

Cover - shares	6 Months Ended
	Jun. 30, 2020	Aug. 03, 2020
Cover [Abstract]
Entity Registrant Name	ADMA BIOLOGICS, INC.
Entity Central Index Key	0001368514
Document Type	10-Q
Amendment Flag	false
Current Fiscal Year End Date	--12-31
Entity Small Business	true
Entity Shell Company	false
Entity Emerging Growth Company	false
Entity Current Reporting Status	Yes
Document Period End Date	Jun. 30, 2020
Entity Filer Category	Accelerated Filer
Document Fiscal Period Focus	Q2
Document Fiscal Year Focus	2020
Entity Common Stock Shares Outstanding		86,349,981
Document Quarterly Report	true
Document Transition Report	false
Entity Interactive Data Current	Yes
Entity File Number	001-36728
Entity Tax Identification Number	56-2590442
Entity Address Postal Zip Code	07446
Entity Incorporation State Country Code	DE
Entity Address Address Line 1	465 State Route 17,
Entity Address City Or Town	Ramsey
Entity Address State Or Province	NJ
Local Phone Number	478-5552
City Area Code	201
Trading Symbol	ADMA
Security Exchange Name	NASDAQ
Security 12b Title	Common Stock

CONDENSED CONSOLIDATED BALANCE

CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
Current assets:
Cash and cash equivalents	$ 75,781,122	$ 26,752,135
Accounts receivable, net	6,514,165	3,469,919
Inventories	56,001,348	53,064,734
Prepaid expenses and other current assets	4,693,427	2,533,593
Total current assets	142,990,062	85,820,381
Property and equipment, net	37,373,366	31,741,317
Intangible assets, net	2,801,797	3,159,474
Goodwill	3,529,509	3,529,509
Deposits and other assets	4,846,834	2,840,044
TOTAL ASSETS	191,541,568	127,090,725
Current liabilities:
Accounts payable	6,909,659	9,174,591
Accrued expenses and other current liabilities	5,616,666	4,481,395
Current portion of deferred revenue	142,834	142,834
Current portion of lease obligations	210,870	229,073
Total current liabilities	12,880,029	14,027,893
Senior notes payable, net of discount	81,648,187	68,291,163
Deferred revenue, net of current portion	2,190,115	2,261,532
Subordinated note payable, net of discount	14,925,760	14,908,053
Lease obligations, net of current portion	2,937,292	1,302,361
Other non-current liabilities	80,730	106,574
TOTAL LIABILITIES	114,662,113	100,897,576
COMMITMENTS AND CONTINGENCIES	0	0
STOCKHOLDERS' EQUITY
Preferred Stock, $0.0001 par value, 10,000,000 shares authorized, no shares issued and outstanding	0	0
Common Stock, $0.0001 par value, 150,000,000 shares authorized, 86,349,981 and 59,318,355 shares issued and outstanding	8,635	5,932
Additional paid-in capital	381,010,696	290,903,772
Accumulated deficit	(304,139,876)	(264,716,555)
TOTAL STOCKHOLDERS' EQUITY	76,879,455	26,193,149
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY	$ 191,541,568	$ 127,090,725

CONDENSED CONSOLIDATED BALANC_2

CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited) (Parenthetical) - $ / shares	Jun. 30, 2020	Dec. 31, 2019
STOCKHOLDERS' EQUITY
Preferred stock, shares par value	$ 0.0001	$ 0.0001
Preferred stock, shares authorized	10,000,000	10,000,000
Preferred stock, shares issued	0	0
Preferred stock, shares outstanding	0	0
Common stock, shares par value	$ 0.0001	$ 0.0001
Common stock, shares authorized	150,000,000	150,000,000
Common stock, shares issued	86,349,981	59,318,355
Common stock, shares outstanding	86,349,981	59,318,355

CONDENSED CONSOLIDATED STATEMEN

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited) - USD ($)	3 Months Ended		6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
REVENUES:
Product revenue	$ 7,751,885	$ 6,525,233	$ 17,915,921	$ 10,018,114
License revenue	35,709	35,709	71,417	71,417
Total Revenues	7,787,594	6,560,942	17,987,338	10,089,531
OPERATING EXPENSES:
Cost of product revenue (exclusive of amortization expense shown below)	13,495,629	10,491,236	30,324,855	19,896,415
Research and development	1,656,420	516,986	3,185,158	1,387,621
Plasma center operating expenses	877,902	594,113	1,378,546	1,248,599
Amortization of intangible assets	178,838	211,234	357,676	422,469
Selling, general and administrative	8,702,630	6,086,047	16,634,714	11,681,517
Total operating expenses	24,911,419	17,899,616	51,880,949	34,636,621
LOSS FROM OPERATIONS	(17,123,825)	(11,338,674)	(33,893,611)	(24,547,090)
OTHER INCOME (EXPENSE):
Interest and other income	19,411	209,808	267,479	337,207
Interest expense	(3,067,306)	(2,072,578)	(5,784,397)	(3,613,085)
Loss on extinguishment of debt	0	0	0	(9,962,495)
Gain on transfer of plasma center assets	0	0	0	11,527,421
Other expense, net	(6,371)	(10,428)	(12,792)	(21,785)
Other expense, net	(3,054,266)	(1,873,198)	(5,529,710)	(1,732,737)
NET LOSS	$ (20,178,091)	$ (13,211,872)	$ (39,423,321)	$ (26,279,827)
BASIC AND DILUTED LOSS PER COMMON SHARE	$ (0.23)	$ (0.25)	$ (0.49)	$ (0.53)
WEIGHTED AVERAGE COMMON SHARES OUTSTANDING: Basic and Diluted	86,347,467	52,206,204	80,064,641	49,295,805

CONDENSED CONSOLIDATED STATEM_2

CONDENSED CONSOLIDATED STATEMENT OF CHANGES IN STOCKHOLDERS' EQUITY (Unaudited) - USD ($)	Total	Common Stock	Additional Paid-In Capital	Accumulated Deficit
Balance, shares at Dec. 31, 2018		46,353,068
Balance, amount at Dec. 31, 2018	$ 19,770,438	$ 4,635	$ 236,203,041	$ (216,437,238)
Stock-based compensation	637,263	0	637,263	0
Warrants issued in connection with note payable	2,699,208	0	2,699,208	0
Net loss	(13,067,955)	$ 0	0	(13,067,955)
Balance, shares at Mar. 31, 2019		46,353,068
Balance, amount at Mar. 31, 2019	10,038,954	$ 4,635	239,539,512	(229,505,193)
Balance, shares at Dec. 31, 2018		46,353,068
Balance, amount at Dec. 31, 2018	19,770,438	$ 4,635	236,203,041	(216,437,238)
Net loss	(26,279,827)
Balance, shares at Jun. 30, 2019		59,317,806
Balance, amount at Jun. 30, 2019	46,905,861	$ 5,932	289,616,994	(242,717,065)
Balance, shares at Mar. 31, 2019		46,353,068
Balance, amount at Mar. 31, 2019	10,038,954	$ 4,635	239,539,512	(229,505,193)
Stock-based compensation	726,736	$ 0	726,736	0
Issuance of common stock, net of offering expenses, shares		12,937,500
Warrants issued in connection with note payable	879,907	$ 0	879,907	0
Issuance of common stock, net of offering expenses, amount	48,397,088	1,294	48,395,794	0
Net loss	(13,211,872)	$ 0	0	(13,211,872)
Exercise of stock options, shares		27,238
Exercise of stock options, amount	75,048	$ 3	75,045	0
Balance, shares at Jun. 30, 2019		59,317,806
Balance, amount at Jun. 30, 2019	46,905,861	$ 5,932	289,616,994	(242,717,065)
Balance, shares at Dec. 31, 2019		59,318,355
Balance, amount at Dec. 31, 2019	26,193,149	$ 5,932	290,903,772	(264,716,555)
Stock-based compensation	676,548	$ 0	676,548	0
Issuance of common stock, net of offering expenses, shares		27,025,000
Issuance of common stock, net of offering expenses, amount	88,704,039	$ 2,703	88,701,336	0
Net loss	(19,245,230)	$ 0	0	(19,245,230)
Exercise of stock options, shares		1,958
Exercise of stock options, amount	7,177	$ 0	7,177	0
Balance, shares at Mar. 31, 2020		86,345,313
Balance, amount at Mar. 31, 2020	96,335,683	$ 8,635	380,288,833	(283,961,785)
Balance, shares at Dec. 31, 2019		59,318,355
Balance, amount at Dec. 31, 2019	26,193,149	$ 5,932	290,903,772	(264,716,555)
Net loss	(39,423,321)
Balance, shares at Jun. 30, 2020		86,349,981
Balance, amount at Jun. 30, 2020	76,879,455	$ 8,635	381,010,696	(304,139,876)
Balance, shares at Mar. 31, 2020		86,345,313
Balance, amount at Mar. 31, 2020	96,335,683	$ 8,635	380,288,833	(283,961,785)
Stock-based compensation	715,608	0	715,608	0
Net loss	(20,178,091)	$ 0	0	(20,178,091)
Exercise of stock options, shares		4,668
Exercise of stock options, amount	6,255	$ 0	6,255	0
Balance, shares at Jun. 30, 2020		86,349,981
Balance, amount at Jun. 30, 2020	$ 76,879,455	$ 8,635	$ 381,010,696	$ (304,139,876)

CONDENSED CONSOLIDATED STATEM_3

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited) - USD ($)	6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019
CASH FLOWS FROM OPERATING ACTIVITIES:
Net loss	$ (39,423,321)	$ (26,279,827)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization	1,674,490	1,611,422
Loss on disposal of fixed assets	3,518	8,788
Stock-based compensation	1,392,156	1,363,999
Gain on transfer of plasma center assets	0	(11,527,421)
Amortization of debt discount	874,732	340,481
Loss on extinguishment of debt	0	9,962,495
Amortization of license revenue	(71,417)	(71,417)
Changes in operating assets and liabilities, net of acquisition:
Accounts receivable	(3,044,246)	(3,694,222)
Inventories	(2,936,614)	(5,175,148)
Prepaid expenses and other current assets	(2,159,834)	163,747
Deposits and other assets	(283,195)	118,832
Accounts payable	(2,264,932)	887,753
Accrued expenses	399,295	(529,589)
Other current and non-current liabilities	(92,067)	(91,029)
Net cash used in operating activities	(45,931,435)	(32,911,136)
CASH FLOWS FROM INVESTING ACTIVITIES:
Purchase of property and equipment	(6,243,284)	(245,675)
Proceeds from the sale of property and equipment	2,000	0
Net cash used in investing activities	(6,241,284)	(245,675)
CASH FLOWS FROM FINANCING ACTIVITIES:
Principal payments on notes payable	0	(30,000,000)
Payment of end of term fee	0	(2,760,000)
Payment of debt refinancing fees	0	(6,499,867)
Proceeds from issuance of note payable	12,500,000	72,500,000
Payment of debt issuance costs	0	(1,679,661)
Proceeds from the issuance of common stock, net of offering expenses	88,704,039	48,397,088
Proceeds from the exercise of stock options	13,432	75,048
Payments on finance lease obligations	(15,765)	14,740
Net cash provided by financing activities	101,201,706	80,017,868
Net increase in cash and cash equivalents	49,028,987	46,861,057
Cash and cash equivalents, including restricted cash - beginning of period	26,752,135	26,754,852
Cash and cash equivalents - end of period	$ 75,781,122	$ 73,615,909

ORGANIZATION AND BUSINESS

ORGANIZATION AND BUSINESS	6 Months Ended
	Jun. 30, 2020
ORGANIZATION AND BUSINESS
1. ORGANIZATION AND BUSINESS	1. ORGANIZATION AND BUSINESS ADMA Biologics, Inc. (“ADMA” or the “Company”) is an end-to-end commercial biopharmaceutical company dedicated to manufacturing, marketing and developing specialty plasma-derived biologics for the treatment of immunodeficient patients at risk for infection and others at risk for certain infectious diseases. The Company’s targeted patient populations include immune-compromised individuals who suffer from an underlying immune deficiency disorder or who may be immune-suppressed for medical reasons. ADMA operates through its wholly-owned subsidiaries ADMA BioManufacturing, LLC (“ADMA BioManufacturing”) and ADMA BioCenters Georgia Inc. (“ADMA BioCenters”). ADMA BioManufacturing was formed in January 2017 to facilitate the acquisition of the Biotest Therapy Business Unit (“BTBU”) from BPC Plasma, Inc. (formerly Biotest Pharmaceuticals Corporation) (“BPC” and, together with Biotest AG, “Biotest”) as more fully described below. BTBU had been the Company’s third-party manufacturer for its then-lead pipeline product candidate, ASCENIV, previously referred to as “RI-002.” ADMA BioCenters is the Company’s source plasma collection business with a plasma collection facility located in the U.S., which holds an approved license with the U.S. Food and Drug Administration (the “FDA”). The Company has three FDA-approved products, all of which are currently marketed and commercially available: (i) BIVIGAM (Immune Globulin Intravenous, Human), an Intravenous Immune Globulin (“IVIG”) product indicated for the treatment of Primary Humoral Immunodeficiency (“PI”), also known as Primary Immunodeficiency Disease (“PIDD”), and for which we received FDA approval on May 9, 2019 for the commercial re-launch of the product and commenced the commercial re-launch in August 2019; (ii) ASCENIV (Immune Globulin Intravenous, Human – slra 10% Liquid), an IVIG product indicated for the treatment of PI, for which we received FDA approval on April 1, 2019 and commenced first commercial sales in October 2019; and (iii) Nabi-HB (Hepatitis B Immune Globulin, Human), which is indicated for the treatment of acute exposure to blood containing Hepatitis B surface antigen (“HBsAg”) and other listed exposures to Hepatitis B. In addition to its commercially available immunoglobulin products, the Company provides contract manufacturing services for certain clients and generates revenues from the sale of intermediate by-products that result from the immunoglobulin production process. The Company seeks to develop a pipeline of plasma-derived therapeutics, and its products and product candidates are intended to be used by physician specialists focused on caring for immune-compromised patients with or at risk for certain infectious diseases. On June 6, 2017, ADMA completed the acquisition of certain assets (the “Biotest Assets”) of BTBU, which included the FDA-licensed BIVIGAM and Nabi-HB immunoglobulin products, and an FDA-licensed plasma fractionation manufacturing facility located in Boca Raton, FL (the “Boca Facility”) (the “Biotest Transaction”). As of June 30, 2020, the Company had working capital of $130.1 million, including $75.8 million of cash and cash equivalents. Based upon the Company’s current projected revenue and expenditures, including capital expenditures and continued implementation of the Company’s commercialization and expansion activities, as well as certain other assumptions, the Company’s management currently believes that its cash, cash equivalents, projected revenue and accounts receivable will be sufficient to fund ADMA’s operations, as currently conducted, into the second quarter of 2021. In order to have sufficient cash to fund its operations thereafter, the Company anticipates it will need to raise additional capital before the end of the second quarter of 2021. These estimates may change based upon several factors, including the success of the Company’s commercial sales of its products, manufacturing ramp-up activities, the acceptability of ADMA’s immune globulin products by physicians, patients or payers and the various financing options that may be available to the Company. In addition, the Company’s end-to-end production cycle from procurement of raw materials to commercial release of finished product can take between seven and 12 months, requiring substantial investments in raw material plasma and other manufacturing materials. The Company currently has no firm commitments for additional financing, and there can be no assurance that the Company will be able to secure additional financing on terms that are acceptable to the Company, or at all. Furthermore, if the Company’s assumptions underlying its estimated expenses and revenues are incorrect, it may have to raise additional capital sooner than currently anticipated. Due to numerous risks and uncertainties associated with FDA approvals related to the Company’s products or the labeled indications of such products, ongoing compliance requirements and capacity expansion efforts at the Company’s Boca Facility and future commercialization of the Company’s products, including the Company’s ability to obtain adequate quantities of FDA-approved plasma with proper specifications on acceptable terms for use in the Company’s manufacturing process, as well as the additional uncertainties surrounding the COVID-19 pandemic (see Note 9) the Company is unable to estimate with certainty the amounts of increased capital outlays and operating expenditures required to fund its commercial and development activities. The Company’s current estimates may be subject to change as circumstances regarding its business requirements evolve. Failure to secure any necessary financing in a timely manner and on commercially reasonable terms could have a material adverse effect on the Company’s business plan and financial performance and it could be forced to delay or discontinue its commercialization, product development or clinical activities or delay or discontinue the approval efforts for any of the Company’s products or product candidates. The Company has reported cumulative losses since inception in June 2004 through June 30, 2020 of $304.1 million. As such, these factors raise substantial doubt about the Company’s ability to continue as a going concern. The accompanying consolidated financial statements do not include any adjustments related to the recoverability and classification of asset carrying amounts and the classification of liabilities that might be necessary from the outcome of this uncertainty. The Company may decide to raise capital through public or private equity offerings or debt financings, or obtain a bank credit facility or enter into corporate collaboration and licensing arrangements. The sale of additional equity or debt securities, if convertible, could result in dilution to the Company’s existing stockholders and, in such event, the market value of its common stock may decline. The incurrence of additional indebtedness would result in increased fixed obligations and could also result in covenants that would restrict the Company’s operations or other financing alternatives. In addition, the Company is exploring additional contract manufacturing arrangements and other business development opportunities, which may provide additional liquidity to the Company. There can be no assurance that the Company’s approved products will be commercially viable, or that research and development, plant capacity expansion, plasma center build-outs or other capital improvements will be successfully completed or that any product developed in the future will be approved. The Company is subject to risks common to companies in the biotechnology and pharmaceutical manufacturing industries including, but not limited to, dependence on collaborative arrangements, development by the Company or its competitors of new technological innovations, dependence on key personnel, protection of proprietary technology, and compliance with FDA and other governmental regulations and approval requirements.

SUMMARY OF SIGNIFICANT ACCOUNTI

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES	6 Months Ended
	Jun. 30, 2020
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
2. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES	2. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES Basis of presentation The accompanying unaudited condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“U.S. GAAP”) for interim financial information. Any reference in these notes to applicable guidance is meant to refer to U.S. GAAP as found in the Accounting Standards Codification (“ASC”) and Accounting Standards Updates (“ASU”) of the Financial Accounting Standards Board (the “FASB”). The accompanying unaudited condensed consolidated financial statements should be read in conjunction with the annual audited consolidated financial statements and notes thereto as of and for the year ended December 31, 2019 included in the Company’s Annual Report on Form 10-K filed with the U.S. Securities and Exchange Commission (the “SEC”) on March 13, 2020.The accompanying consolidated balance sheet as of December 31, 2019 was derived from the audited financial statements for the year ended December 31, 2019. These condensed consolidated interim financial statements have been prepared in accordance with the instructions to Form 10-Q and Article 8 of Regulation S-X, and therefore omit or condense certain footnotes and other information normally included in complete consolidated financial statements prepared in accordance with U.S. GAAP. All intercompany balances and transactions have been eliminated in consolidation. In the opinion of management, the accompanying unaudited condensed consolidated financial statements include all normal and recurring adjustments (which consist primarily of accruals, estimates and assumptions that impact the financial statements) considered necessary to present fairly the Company’s financial position as of June 30, 2020 and its results of operations, changes in equity and cash flows for the three and six months ended June 30, 2020. During the three and six months ended June 30, 2020 and 2019, comprehensive loss was equal to the net loss amounts presented for the respective periods in the accompanying condensed consolidated statements of operations. Operating results for interim periods are not necessarily indicative of the results that may be expected for the full fiscal year. Use of estimates The preparation of financial statements requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates. Significant estimates include the realizable value of accounts receivable, valuation of inventory, assumptions used in projecting future liquidity and capital requirements, assumptions used in the fair value of awards granted under the Company’s equity incentive plans and warrants issued in connection with the issuance of notes payable and the valuation allowance for the Company’s deferred tax assets. Fair value of financial instruments The carrying amounts of certain of the Company’s financial instruments, including cash and cash equivalents, accounts receivable and accounts payable, are shown at cost which approximates fair value due to the short-term nature of these instruments. The debt outstanding under the Company’s senior secured term loan (see Note 6) approximates fair value due to the variable interest rate on this debt. With respect to the subordinated note payable in the amount of $15.0 million as of June 30, 2020 and December 31, 2019 held by Biotest, a principal stockholder of the Company at the time the note was issued concurrent with an acquisition transaction with an affiliate of such stockholder (see Note 6), the Company has concluded that an estimation of fair value for this note is not practicable. Accounts receivable Accounts receivable is reported at realizable value, net of allowances for contractual credits and doubtful accounts, which are recognized in the period the related revenue is recorded. The Company extends credit to its customers based upon an evaluation of each customer's financial condition and credit history. Evaluations of the financial condition and associated credit risk of customers are performed on an ongoing basis. Based on these evaluations, the Company has concluded that its credit risk is minimal. At June 30, 2020, three customers accounted for an aggregate of 76% of the Company’s total accounts receivable, and at December 31, 2019, two customers accounted for 89% of the Company’s total accounts receivable. Inventories Inventories, including plasma intended for resale and plasma intended for internal use in the Company’s manufacturing, commercialization or research and development activities, are carried at the lower of cost or net realizable value determined by the first-in, first-out method. Due to previous uncertainties surrounding certain prior submissions made to the FDA, all costs related to the production of BIVIGAM and ASCENIV prior to their FDA approval dates of May 9, 2019 and April 1, 2019, respectively, have been charged to cost of product revenue in the accompanying consolidated statements of operations during the period the product was produced. In addition, costs associated with the production of conformance or engineering lots that would not qualify as immediately available for commercial sale are charged to cost of product revenue and not capitalized into inventory. Goodwill Goodwill represents the excess of purchase price over the fair value of net assets acquired by the Company. Goodwill at June 30, 2020 and December 31, 2019 was $3.5 million. All of the Company’s goodwill is attributable to its ADMA BioManufacturing business segment and is related to a 2017acquisition transaction. Goodwill is not amortized, but is assessed for impairment on an annual basis or more frequently if impairment indicators exist. The Company has the option to perform a qualitative assessment of goodwill to determine whether it is more likely than not that the fair value of its reporting unit is less than its carrying amount, including goodwill and other intangible assets. If the Company concludes that this is the case, then it must perform a goodwill impairment test by comparing the fair value of the reporting unit to its carrying value. An impairment charge is recorded to the extent the reporting unit’s carrying value exceeds its fair value, not to exceed the total amount of goodwill allocated to that reporting unit. The Company performs its annual goodwill impairment test as of October 1 of each year. The Company’s annual goodwill impairment test as of October 1, 2019 did not result in a goodwill impairment charge, and the Company did not record any impairment charges related to goodwill for the three and six months ended June 30, 2020 and 2019. Impairment of long-lived assets The Company assesses the recoverability of its long-lived assets, which include property and equipment and definite-lived intangible assets, whenever significant events or changes in circumstances indicate impairment may have occurred. If indicators of impairment exist, projected future undiscounted cash flows associated with the asset are compared to its carrying amount to determine whether the asset’s carrying value is recoverable. Any resulting impairment is recorded as a reduction in the carrying value of the related asset in excess of fair value and a charge to operating results. For the three and six months ended June 30, 2020 and 2019, the Company determined that there was no impairment of its long-lived assets. Revenue recognition Revenues for the three and six months ended June 30, 2020 and 2019 are comprised of (i) revenues from the sale of the Company’s immunoglobulin products, ASCENIV, BIVIGAM and Nabi-HB, (ii) product revenues from the sale of human plasma collected through the Company’s Plasma Collection Centers business segment, (iii) contract manufacturing revenue, (iv) revenues from the sale of intermediate by-products; and (v) license and other revenues primarily attributable to the out-licensing of ASCENIV to Biotest in 2012 to market and sell this product in Europe and selected countries in North Africa and the Middle East. Biotest has provided the Company with certain services and financial payments in accordance with the related Biotest license agreement and is obligated to pay the Company certain amounts in the future if certain milestones are achieved. Deferred revenue is amortized into income over the term of the Biotest license, representing a period of approximately 22 years. Product revenue is recognized when the customer is deemed to have control over the product. Control is determined based on when the product is shipped or delivered and title passes to the customer. Revenue is recorded in an amount that reflects the consideration the Company expects to receive in exchange. Revenue from the sale of the Company’s immunoglobulin products is recognized when the product reaches the customer’s destination, and is recorded net of estimated rebates, price protection arrangements and customer incentives, including prompt pay discounts, wholesaler chargebacks and other wholesaler fees. These estimates are based on historical experience and certain other assumptions, and the Company believes that such estimates are reasonable. For revenues associated with contract manufacturing and the sale of intermediates, control transfers to the customer and the performance obligation is satisfied when the customer takes possession of the product from the Boca Facility or from a third-party warehouse that is utilized by the Company. Product revenues from the sale of human plasma collected at the Company’s plasma collection centers are recognized at the time control of the product has been transferred to the customer, which generally occurs at the time of shipment. Product revenues are recognized at the time of delivery if the Company retains control of the product during shipment. For the six months ended June 30, 2020, three customers represented an aggregate of 81% of the Company’s consolidated revenues. For the six months ended June 30, 2019, three customers represented an aggregate of 84% of the Company’s consolidated revenues. Cost of product revenue Cost of product revenue includes costs associated with the manufacture of the Company’s FDA approved products, intermediates and the sale of human source plasma, as well as expenses related to conformance batch production, process development and scientific and technical operations when these operations are attributable to marketed products. When the activities of these operations are attributable to new products in development, the expenses are classified as research and development expenses. Loss per common share Basic loss per common share is computed by dividing net loss attributable to common stockholders by the weighted average number of shares of common stock outstanding during the period. Diluted loss per common share is calculated by dividing net loss attributable to common stockholders, as adjusted for the effect of dilutive securities, if any, by the weighted average number of shares of common stock and dilutive common stock outstanding during the period. Potentially dilutive common stock includes the shares of common stock issuable upon the exercise of outstanding stock options and warrants, using the treasury stock method. Potentially dilutive common stock is excluded from the diluted loss per common share computation to the extent that it would be anti-dilutive. As a result, no potentially dilutive securities are included in the computation of any of the accompanying diluted loss per share amounts as the Company reported a net loss for all periods presented. For the six months ended June 30, 2020 and 2019, the following securities were excluded from the calculation of diluted loss per common share because of their anti-dilutive effects: For the Six Months Ended June 30, 2020 2019 Stock options 6,801,779 5,624,603 Restricted stock units 326,000 - Warrants 2,138,160 2,138,160 9,265,939 7,762,763 Stock-based compensation The Company follows recognized accounting guidance which requires all equity-based payments, including grants of stock options, to be recognized in the statement of operations as compensation expense based on their fair values at the date of grant. Compensation expense related to awards to employees and directors with service-based vesting conditions is recognized on a straight-line over the associated vesting period of the award based on the grant date fair value of the award. Stock options granted under the Company’s equity incentive plans generally have a four-year vesting period and a term of 10 years. Pursuant to ASU No. 2016-09, Improvements to Employee Share-Based Payment Accounting (Topic 718) Income Taxes The Company recognizes deferred tax assets and liabilities for the expected future tax consequences of events that have been included in the consolidated financial statements or its tax returns. Under this method, deferred tax assets and liabilities are recognized for the temporary differences between the tax bases of assets and liabilities and their respective financial reporting amounts at enacted tax rates in effect for the years in which the temporary differences are expected to reverse. The Company records a valuation allowance on its deferred tax assets if it is more likely than not that the Company will not generate sufficient taxable income to utilize its deferred tax assets. The Company is subject to income tax examinations by major taxing authorities for all tax years since 2015 and for previous periods as it relates to the Company’s net operating loss carryforwards. In accordance with U.S. GAAP, the Company is required to determine whether a tax position of the Company is more likely than not to be sustained upon examination by the applicable taxing authority, including resolution of any related appeals or litigation processes, based on the technical merits of the position. The tax benefit to be recognized is measured as the largest amount of benefit that is greater than fifty percent likely of being realized upon ultimate settlement. Derecognition of a tax benefit previously recognized could result in the Company recording a tax liability that would reduce net assets. Based on its analysis, the Company has determined that it has not incurred any liability for unrecognized tax benefits as of June 30, 2020 and December 31, 2019, and during the three and six months ended June 30, 2020 and 2019, the Company recognized no adjustments for uncertain tax positions. Recent Accounting Pronouncements In June 2016, the FASB issued ASU No. 2016-13, Financial Instruments – Credit Losses (Topic 326) In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842) In July 2017, the FASB issued ASU No. 2017-11, Earnings Per Share (Topic 260), Distinguishing Liabilities from Equity (Topic 480), Derivatives and Hedging (Topic 815)

INVENTORIES

INVENTORIES	6 Months Ended
	Jun. 30, 2020
INVENTORIES
3. INVENTORIES	3. INVENTORIES The following table provides the components of inventories: June 30, December 31, Raw materials $ 24,830,796 $ 33,381,806 Work-in-progress 22,066,417 14,455,665 Finished goods 9,104,135 5,227,263 Total inventories $ 56,001,348 $ 53,064,734 Raw materials includes plasma and other materials expected to be used in the production of ASCENIV, BIVIGAM and Nabi-HB, as there are alternative uses for these materials that provide a probable future benefit or will be consumed in the production of goods expected to be available for sale. All other activities and materials associated with the production of inventories used in research and development activities are expensed as incurred. Work-in-process inventory primarily consists of bulk drug substance and unlabeled filled vials of the Company’s immunoglobulin products. Finished goods inventory is comprised of immunoglobulin product inventory and related intermediates that are available for commercial sale, as well as plasma collected at the Company’s plasma collection center which is expected to be sold to third-party customers.

INTANGIBLE ASSETS

INTANGIBLE ASSETS	6 Months Ended
	Jun. 30, 2020
INTANGIBLE ASSETS
4. INTANGIBLE ASSETS	4. INTANGIBLE ASSETS Intangible assets at June 30, 2020 and December 31, 2019 consist of the following: June 30, 2020 December 31, 2019 Accumulated Accumulated Cost Amortization Net Cost Amortization Net Trademark and other intangible rights related to Nabi-HB $ 4,100,046 $ 1,805,973 $ 2,294,073 $ 4,100,046 $ 1,513,112 $ 2,586,934 Rights to intermediates 907,421 399,697 507,724 907,421 334,881 572,540 Customer contract 1,076,557 1,076,557 - 1,076,557 1,076,557 - $ 6,084,024 $ 3,282,227 $ 2,801,797 $ 6,084,024 $ 2,924,550 $ 3,159,474 All of the Company’s intangible assets were acquired in the Biotest Transaction. Amortization expense related to these intangible assets for the three months ended June 30, 2020 and 2019 was $0.2 million, and amortization expense for the six months ended June 30, 2020 and 2019 was $0.4 million. Estimated aggregate future aggregate amortization expense for the next five years is expected to be as follows: Remainder of 2020 $ 357,676 2021 715,352 2022 715,352 2023 715,352 2024 298,065

PROPERTY AND EQUIPMENT

PROPERTY AND EQUIPMENT	6 Months Ended
	Jun. 30, 2020
PROPERTY AND EQUIPMENT
5. PROPERTY AND EQUIPMENT	5. PROPERTY AND EQUIPMENT Property and equipment and related accumulated depreciation are summarized as follows: June 30, 2020 December 31, 2019 Manufacturing and laboratory equipment $ 9,898,186 $ 8,831,817 Office equipment and computer software 2,220,856 1,690,248 Furniture and fixtures 1,400,129 582,088 Construction in process 6,672,211 4,285,915 Leasehold improvements 3,011,009 1,673,084 Land 4,339,441 4,339,441 Buildings and building improvements 16,869,821 16,063,680 44,411,653 37,466,273 Less: Accumulated depreciation (7,038,287 ) (5,724,956 ) Total property and equipment, net $ 37,373,366 $ 31,741,317 Fixed assets are stated at cost less accumulated depreciation. Depreciation is calculated using the straight-line method over the asset’s estimated useful life. Land is not depreciated. The buildings were assigned a useful life of 30 years. Property and equipment other than land and buildings have useful lives ranging from three to 10 years. Leasehold improvements are amortized over the lesser of the lease term or their estimated useful lives. The Company recorded depreciation expense on property and equipment for the three and six months ended June 30, 2020 of $0.7 million and $1.3 million, respectively. Depreciation expense for the three and six months ended June 30, 2019 was $0.6 million and $1.2 million, respectively.

DEBT

DEBT	6 Months Ended
	Jun. 30, 2020
DEBT
6. DEBT	6. DEBT Senior Notes Payable A summary of outstanding senior notes payable is as follows: June 30, 2020 December 31, 2019 Notes payable $ 85,000,000 $ 72,500,000 Less: Debt discount (3,351,813 ) (4,208,837 ) Senior notes payable $ 81,648,187 $ 68,291,163 On February 11, 2019 (the “Perceptive Closing Date”), the Company and all of its subsidiaries entered into a Credit Agreement and Guaranty (the “Perceptive Credit Agreement”) with Perceptive Credit Holdings II, LP, as the lender and administrative agent (“Perceptive”). The Perceptive Credit Agreement, as amended, provides for a senior secured term loan facility in a principal amount of up to $85.0 million (the “Perceptive Credit Facility”), comprised of (i) a term loan made on the Perceptive Closing Date in the principal amount of $45.0 million, as evidenced by the Company’s issuance of a promissory note (the “Perceptive Tranche I Note”) in favor of Perceptive on the Perceptive Closing Date (the “Perceptive Tranche I Loan”), (ii) a term loan in the principal amount of up to $27.5 million (the “Perceptive Tranche II Loan”) evidenced by the Company’s issuance of a promissory note (the “Perceptive Tranche II Note”) in favor of Perceptive on May 3, 2019; and (iii) a term loan in the principal amount of up to $12.5 million evidenced by the Company’s issuance of a promissory note (the “Perceptive Tranche III Note”) in favor of Perceptive on March 20, 2020 (the “Perceptive Tranche III Loan,” and together with the Perceptive Tranche I Loan and the Perceptive Tranche II Loan, the “Perceptive Loans”). The Perceptive Tranche III Loan is the result of an amendment to the Perceptive Credit Agreement (the “Perceptive Amendment”) that the Company and Perceptive entered into on May 3, 2019, and the Perceptive Tranche III Loan became available to the Company upon the approval of BIVIGAM on May 9, 2019. The Perceptive Credit Facility has a maturity date of March 1, 2022 (the “Maturity Date”), subject to acceleration pursuant to the Perceptive Credit Agreement, including upon an Event of Default (as defined in the Perceptive Credit Agreement). On the Perceptive Closing Date, the Company used $30.0 million of the Perceptive Tranche I Loan to terminate and pay in full all of the outstanding obligations under its previously existing credit agreement with Marathon Healthcare Finance Fund, L.P. (“Marathon”) (the “Marathon Credit Facility”). The Company also used proceeds from the Perceptive Tranche I Loan to: (i) pay a deferred facility fee to Marathon in the amount of $2.8 million, (ii) pay a prepayment penalty to Marathon in the amount of $6.5 million, (iii) pay outstanding accrued interest to Marathon in the amount of $0.7 million, and (iv) pay certain fees and expenses incurred in connection with the Perceptive Credit Facility of approximately $1.5 million. In addition, Marathon released $4.0 million of cash to the Company that was held in a debt service reserve account per the terms of the Marathon Credit Facility. In connection with the Perceptive Amendment, the Company paid an additional facility fee to Perceptive in the amount of $0.1 million on May 3, 2019. As a result of the Company’s entering into the Perceptive Credit Agreement and terminating the Marathon Credit Facility, the Company recognized a loss on the extinguishment of debt for the six months ended June 30, 2019 in the amount of approximately $10.0 million, comprised of the $6.5 million prepayment penalty and the write-off of unamortized debt discount related to the Marathon Credit Facility in the amount of $3.5 million. Borrowings under the Perceptive Credit Agreement bear interest at a rate per annum equal to 7.5% plus the greater of (i) one-month LIBOR and (ii) 3.5%; provided, however, that upon, and during the continuance of, an Event of Default, the interest rate will automatically increase by an additional 400 basis points. Accrued interest is payable to Perceptive on the last day of each month during the term of the Perceptive Credit Facility.The rate of interest in effect as of the Perceptive Closing Date and at June 30, 2020 was 11.0%. On the Maturity Date, the Company will pay Perceptive the entire outstanding principal amount underlying the Perceptive Loans and any accrued and unpaid interest thereon. Prior to the Maturity Date, there will be no scheduled principal payments on the Perceptive Loans. The Company may prepay outstanding principal on the Perceptive Loans at any time and from time to time upon three business days’ prior written notice, subject to the payment to Perceptive of (A) any accrued but unpaid interest on the prepaid principal amount plus (B) a redemption premium amount equal to (i) 5.0% of the prepaid principal amount, if prepaid on or prior to the first anniversary of the Perceptive Closing Date, (ii) 4.0% of the prepaid principal amount, if prepaid after the first anniversary of the Perceptive Closing Date and on or prior to the second anniversary of the Perceptive Closing Date, or (iii) 3.0% of the prepaid principal amount, if prepaid after the second anniversary of the Perceptive Closing Date and on or prior to the third anniversary of the Perceptive Closing Date. All of the Company’s obligations under the Perceptive Credit Agreement are secured by a first-priority lien and security interest in substantially all of the Company’s tangible and intangible assets, including intellectual property and all of the equity interests in the Company’s subsidiaries. The Perceptive Credit Agreement contains certain representations and warranties, affirmative covenants, negative covenants and conditions that are customarily required for similar financings. The negative covenants restrict or limit the ability of the Company and its subsidiaries to, among other things and subject to certain exceptions contained in the Perceptive Credit Agreement, incur new indebtedness; create liens on assets; engage in certain fundamental corporate changes, such as mergers or acquisitions, or changes to the Company’s or its subsidiaries’ business activities; make certain Investments or Restricted Payments (each as defined in the Perceptive Credit Agreement); change its fiscal year; pay dividends; repay other certain indebtedness; engage in certain affiliate transactions; or enter into, amend or terminate any other agreements that have the impact of restricting the Company’s ability to make loan repayments under the Perceptive Credit Agreement. In addition, the Company must (i) at all times prior to the Maturity Date maintain a minimum cash balance of $3.0 million; and (ii) as of the last day of each fiscal quarter commencing with the fiscal quarter ended June 30, 2019, report revenues for the trailing 12-month period that exceed the amounts set forth in the Perceptive Credit Agreement, which range from $7.0 million for the fiscal quarter ended June 30, 2019 to $55.0 million for the fiscal quarter ending December 31, 2021. At June 30, 2020, the Company was in compliance with all of the covenants contained in the Perceptive Credit Agreement. As consideration for the Perceptive Credit Agreement, the Company issued to Perceptive a warrant to purchase 1,360,000 shares of the Company’s common stock (the “Perceptive Warrant”) on the Perceptive Closing Date. The Perceptive Warrant has an exercise price equal to $3.28 per share, which is equal to the trailing 10-day volume weighted average price (“VWAP”) of the Company’s common stock on the business day immediately prior to the Perceptive Closing Date multiplied by 1.15. The Company valued the Perceptive Warrant at $2.7 million as of the Perceptive Closing Date and it has an expiration date of February 11, 2029. In connection with the Perceptive Amendment, the Company issued an additional warrant (the “Perceptive Tranche III Warrant” and, together with the Perceptive Warrant, the “Perceptive Warrants”) to purchase 250,000 shares of the Company’s common stock to Perceptive with an exercise price equal to $4.64 per share, which represents the trailing 10-day VWAP of the Company’s common stock as of May 2, 2019. The Perceptive Tranche III Warrant was valued by the Company at $0.9 million and has an expiration date of May 3, 2029. Perceptive has represented to the Company, among other things, that it was an “accredited investor” (as such term is defined in Rule 501(a) of Regulation D under the Securities Act) and the Company issued the Perceptive Warrants in reliance upon an exemption from registration contained in Section 4(2) under the Securities Act. The Perceptive Warrants and the shares of common stock issuable thereunder may not be offered, sold, pledged or otherwise transferred in the U.S. absent registration or an applicable exemption from the registration requirements under the Securities Act. As a result of the fees paid to Perceptive and the value of the Perceptive Warrants, the Company recognized an aggregate discount on the Perceptive Tranche I Note and Perceptive Tranche II Note in the amount of $5.3 million. The Company records debt discount as a reduction to the face amount of the debt, and the debt discount is amortized as interest expense over the life of the debt using the interest method. Based on the fair value of the Perceptive Warrants and the aggregate amount of fees and expenses associated with obtaining the Perceptive Credit Facility, the effective interest rate on the Perceptive Loans as of May 3, 2019 was approximately 14.1%. Subordinated Note Payable A summary of the outstanding subordinated note payable is as follows: June 30, 2020 December 31, 2019 Subordinated note payable to Biotest $ 15,000,000 $ 15,000,000 Less: Debt discount (74,240 ) (91,947 ) Subordinated note payable $ 14,925,760 $ 14,908,053 In connection with the acquisition of the Biotest Assets (see Note 1), ADMA BioManufacturing issued a subordinated note payable to BPC and in connection therewith received cash proceeds of $15.0 million. This note has since been assigned from BPC to Biotest AG. The note bears interest at a rate of 6.0% per annum and matures on June 6, 2022.The Company is obligated to make semi-annual interest payments, with all principal and unpaid interest due at maturity. The note is subordinate to all amounts outstanding under the Perceptive Credit Agreement. In the event of default, all principal and unpaid interest is due on demand. The subordinated note also contains several non-financial covenants with which the Company was in compliance as of June 30, 2020.

STOCKHOLDERS' EQUITY

STOCKHOLDERS' EQUITY	6 Months Ended
	Jun. 30, 2020
STOCKHOLDERS' EQUITY
7. STOCKHOLDERS' EQUITY	7. STOCKHOLDERS’ EQUITY Preferred Stock The Company is currently authorized to issue up to 10 million shares of preferred stock, $0.0001, par value per share. There were no shares of preferred stock outstanding at June 30, 2020 and December 31, 2019. Common Stock As of June 30, 2020 and December 31, 2019, the Company was authorized to issue 150,000,000 shares of its common stock, $0.0001 par value per share, and 86,349,981 and 59,318,355 shares of common stock were outstanding as of June 30, 2020 and December 31, 2019, respectively. After giving effect to the 9,265,939 shares reserved for outstanding warrants and awards issued under the Company’s equity incentive plans, as of June 30, 2020 there were 54,384,080 shares of common stock available for issuance. On February 11, 2020, the Company completed an underwritten public offering of 23,500,000 shares of its common stock for gross proceeds of $82.3 million. On February 21, 2020, the Company sold an additional 3,525,000 shares pursuant to the underwriters’ exercise of their option to purchase additional shares of the Company’s common stock for additional gross proceeds of $12.3 million. The Company received net proceeds, after underwriting discounts and other expenses associated with the offering, of approximately $88.7 million. Warrants At June 30, 2020 and December 31, 2019, the Company had outstanding warrants to purchase an aggregate of 2,138,160 shares of common stock, with a weighted average exercise price of $3.81 per share and expiration dates ranging between June 2022 and May 2029. Equity Incentive Plans The fair value of stock options granted under the Company’s 2007 Employee Stock Option Plan (the “2007 Plan”) and the ADMA Biologics, Inc. 2014 Omnibus Incentive Compensation Plan, as amended and restated (the “2014 Plan”), was determined on the date of grant using the Black-Scholes option valuation model. The Black-Scholes model was developed for use in estimating the fair value of publicly traded options, which have no vesting restrictions and are fully transferable. In addition, option valuation models require the input of certain subjective assumptions including the expected stock price volatility. The stock options granted to employees and directors have characteristics significantly different from those of traded options, and changes in the subjective input assumptions can materially affect the fair value estimate. The following assumptions were used to determine the fair value of options granted during the six months ended June 30, 2020 and 2019: Six Months Ended June 30, 2020 2019 Expected term 5.5 - 6.3 years 5.8 - 6.3 years Volatility 62%-67% 54%-62% Dividend yield 0.0 0.0 Risk-free interest rate 0.38-1.68% 1.80-2.92% During the six months ended June 30, 2020 and 2019, the Company granted options to purchase an aggregate of 1,232,500 and 1,429,100 shares of common stock, respectively, to its directors, employees and certain third-party service providers. The weighted average remaining contractual life of stock options outstanding and expected to vest at June 30, 2020 is 6.9 years. The weighted average remaining contractual life of stock options exercisable at June 30, 2020 is 5.6 years. A summary of the Company’s option activity under the 2007 Plan and 2014 Plan and related information is as follows: Shares Weighted Average Exercise Price Balance at December 31, 2019 5,630,351 $ 4.76 Forfeited (47,683 ) $ 3.51 Expired (6,763 ) $ 4.34 Granted 1,232,500 $ 2.96 Exercised (6,626 ) $ 2.03 Balance at June 30, 2020 6,801,779 $ 4.45 Options exercisable 4,030,098 $ 5.19 As of June 30, 2020, the Company had $5.1 million of unrecognized compensation expense related to options granted under the Company’s equity incentive plans, which is expected to be recognized over a weighted-average period of 2.6 years. During the six months ended June 30, 2020, the Company granted Restricted Stock Units (“RSUs”) to members of the Company’s Board of Directors and to certain management employees of the Company. The total RSUs granted during the period represent an aggregate of 341,000 shares of the Company’s common stock. The RSUs vest semi-annually over a period of one year for directors and annually over a period of four years for employees. Total compensation expense related to unvested RSUs for the three and six months ended June 30, 2020 was $0.1 million. A summary of the Company’s unvested RSU activity and related information is as follows: Shares Weighted Average Grant Date Fair Value Balance at December 31, 2019 - $ - Granted 341,000 $ 2.80 Vested - $ - Forfeited (15,000 ) $ 2.92 Balance at June 30, 2020 326,000 $ 2.80 As of June 30, 2020, the Company had $0.8 million of unrecognized compensation expense related to unvested RSUs granted under the Company’s equity incentive plans, which is expected to be recognized over a weighted-average period of 3.5 years. Total stock-based compensation expense for all awards granted under the Company’s equity incentive plans for the three and six months ended June 30, 2020 and 2019 is as follows: Three Months Ended June 30, Six Months Ended June 30, 2020 2019 2020 2019 Research and development $ 105,029 $ 89,543 $ 198,603 $ 176,066 Plasma centers 8,510 13,213 15,754 24,753 Selling, general and administrative 539,256 569,349 1,063,145 1,067,820 Cost of product revenue 62,813 54,631 114,654 95,360 Total stock-based compensation expense $ 715,608 $ 726,736 $ 1,392,156 $ 1,363,999

RELATED PARTY TRANSACTIONS

RELATED PARTY TRANSACTIONS	6 Months Ended
	Jun. 30, 2020
RELATED PARTY TRANSACTIONS
8. RELATED PARTY TRANSACTIONS	8. RELATED PARTY TRANSACTIONS The Company leases an office building and equipment from Areth, LLC (“Areth”) pursuant to an agreement for services effective as of January 1, 2016, as amended from time to time. Effective October 1, 2017, monthly rent on this facility was set at $10,000. On November 7, 2019, an additional amendment was entered into between Areth and the Company to extend the term of this agreement through September 30, 2020, and to provide for automatic one-year renewals unless ADMA gives written notice of termination to Areth 60 days prior to the end of the term, which expires each year on September 30. The Company did not provide a written notice of termination to Areth as of July 31, 2020. Rent expense for the six months ended June 30, 2020 and 2019 amounted to $60,000. Areth is a company controlled by Dr. Jerrold B. Grossman, the Vice Chairman of the Company’s Board of Directors, and Adam S. Grossman, the Company’s President and Chief Executive Officer. The Company also reimburses Areth for office and building related (common area) expenses, equipment and certain other operational expenses, which were not material to the consolidated financial statements for the three and six months ended June 30, 2020 and 2019. See Note 6 for a discussion of the Company’s credit facility and related transactions with Perceptive, a holder of more than 10% of the Company’s common stock. In connection with the February 2020 public offering of the Company’s common stock (see Note 7) on February 11, 2020: (i) Perceptive Advisors, a principal stockholder of ADMA, purchased 4,563,700 shares of common stock through one of its affiliates, (ii) Dr. Grossman purchased 22,857 shares of common stock directly and 22,857 shares indirectly through an entity he controls (iii) Lawrence P. Guiheen, a director of the Company, purchased 20,000 shares of common stock, (iv) Mr. Grossman purchased 28,571 shares of common stock directly and 57,143 shares indirectly through an entity he controls (v) Brian Lenz, the Company’s Executive Vice President and Chief Financial Officer, purchased 7,142 shares of common stock, and (vi) James Mond, the Company’s Chief Scientific Officer and Chief Medical Officer, purchased 4,285 shares of common stock, all at the public offering price of $3.50 per share.

COMMITMENT AND CONTINGENCIES

COMMITMENT AND CONTINGENCIES	6 Months Ended
	Jun. 30, 2020
COMMITMENT AND CONTINGENCIES
9. COMMITMENTS AND CONTINGENCIES	9. COMMITMENTS AND CONTINGENCIES General Legal Matters From time to time the Company is or may become subject to certain legal proceedings and claims arising in connection with the normal course of its business. Management does not expect that the outcome of any such claims or actions will have a material effect on the Company’s liquidity, results of operations or financial condition. COVID-19 Pandemic The Company continues to monitor the ongoing developments related to the COVID-19 pandemic, and its impacts to the Company’s supply-chain operations, including procurement of raw materials and packaging materials, a portion of which are sourced internationally, and the testing of finished drug product that is required prior to its availability for commercial sale. A substantial portion of such testing has historically been performed by contract laboratories outside the United States. The Company has experienced some delays with final drug product release testing by third-party vendors. In response to these delays, the Company added additional release testing laboratories to its FDA approved consortium listed in its drug approval documents which the Company believes has adequately addressed this issue. In addition, due to previous state and local “shelter-in-place” orders, the Company experienced lower than normal donor collections at its FDA approved plasma collection center during the three months ended June 30, 2020. The Company was also subject to delays in shipments of source plasma from its contracted third-party suppliers, as well as delays in deliveries for personal protective equipment, reagents and other non-plasma raw materials and supplies used in the manufacture of its products. The COVID-19 pandemic has also impacted, to a certain degree, the Company’s customer engagement initiatives, whereby ADMA’s sales and medical affairs field personnel have faced difficulties communicating directly with physicians and other healthcare professionals, as well as the cancellation or postponement of a number of key scientific and medical meetings, further limiting the Company’s ability to communicate with potential customers. The Company has implemented a comprehensive suite of virtual engagement initiatives, however, clinician engagement has been reduced due to rapidly evolving COVID-19 priorities at U.S. medical centers. Notwithstanding the foregoing, the COVID-19 pandemic to date has not had a material impact on the Company’s financial condition or results of operations, and the Company does not believe that its production operations at the Boca Facility, the Company’s contract fill/finishers or its plasma collection facility have been significantly impacted by the COVID-19 pandemic. As a result, the Company does not anticipate any material impairments with respect to any of its long-lived assets, including the Company’s property and equipment, goodwill or intangible assets. Although the COVID-19 pandemic has not, to date, materially adversely impacted the Company’s capital and financial resources, because the Company is unable to determine the ultimate severity or duration of the pandemic or its long-term effects on, among other things, the global, national or local economies, the capital and credit markets or the Company’s workforce, customers or our suppliers, at this time the Company is unable to predict whether COVID-19 will have a material adverse impact on the Company’s business, financial condition, liquidity and results of operations. Vendor and Licensor Commitments Pursuant to the terms of a plasma purchase agreement with BPC dated as of November 17, 2011 (the “2011 Plasma Purchase Agreement”), the Company agreed to purchase from BPC an annual minimum volume of source plasma containing antibodies to RSV to be used in the manufacture of ASCENIV. The Company must purchase a to-be-determined and agreed upon annual minimum volume from BPC, but may also collect high-titer RSV plasma from up to five wholly-owned ADMA plasma collection facilities. During 2015, the Company and BPC amended the 2011 Plasma Purchase Agreement to allow the Company the ability to collect its raw material RSV high-titer plasma from other third-party collection organizations, thus allowing the Company to expand its reach for raw material supply as it continues its commercialization activities for ASCENIV. Unless terminated earlier, the 2011 Plasma Purchase Agreement expires in June 2027, after which it may be renewed for two additional five-year periods if agreed to by the parties. As part of the closing of the Biotest Transaction, the parties amended the 2011 Plasma Purchase Agreement to extend the initial term through the ten-year anniversary of the closing date of the Biotest Transaction. On December 10, 2018, BPC assigned its rights and obligations under the 2011 Plasma Purchase Agreement to Grifols Worldwide Operations Limited (“Grifols”) as its successor-in-interest, effective January 1, 2019. On January 1, 2019, Grifols and the Company entered into an additional amendment to the 2011 Plasma Purchase Agreement for the purchase of source plasma containing antibodies to RSV from Grifols. Pursuant to this amendment, until January 1, 2022, the Company may purchase RSV plasma from Grifols from the two plasma collection centers that were transferred to BPC on January 1, 2019 at a price equal to cost plus 5% without any additional increase due to inflation. On June 6, 2017, the Company and BPC entered into a Plasma Supply Agreement pursuant to which BPC supplies, on an exclusive basis subject to certain exceptions, to ADMA BioManufacturing an annual minimum volume of hyperimmune plasma that contain antibodies to the hepatitis B virus for the manufacture of Nabi-HB. The Plasma Supply Agreement has a 10-year term. On July 19, 2018, the Company and BPC entered into an amendment to the Plasma Supply Agreement to provide, among other things, that in the event BPC elects not to supply in excess of ADMA BioManufacturing’s specified amount of Hepatitis B plasma and ADMA BioManufacturing is unable to secure Hepatitis B plasma from a third party at a price that is within a low double digit percentage of the price that ADMA BioManufacturing pays to BPC, then BPC shall reimburse ADMA BioManufacturing for the difference in price ADMA BioManufacturing incurs. On December 10, 2018, BPC assigned its rights and obligations under the Plasma Supply Agreement to Grifols, effective January 1, 2019. On June 6, 2017, the Company and BPC entered into a Plasma Purchase Agreement (the “2017 Plasma Purchase Agreement”), pursuant to which ADMA BioManufacturing purchases normal source plasma (“NSP”) from BPC at agreed upon annual quantities and prices. The 2017 Plasma Purchase Agreement had an initial term of five years after which the 2017 Plasma Purchase Agreement may be renewed for two additional terms of two years each upon the mutual written consent of the parties. On July 19, 2018, the Company and BPC entered into an amendment to the 2017 Plasma Purchase Agreement to, among other things, provide agreed upon amounts of NSP to be supplied by BPC to ADMA BioManufacturing in calendar year 2019 at a specified price per liter, provided that ADMA BioManufacturing delivers a valid purchase order to BPC. Additionally, pursuant to the amendment to the 2017 Plasma Purchase Agreement, BPC agrees that, for calendar years 2020 and 2021, it shall supply no less than a high double digit percentage of ADMA BioManufacturing’s requested NSP amounts, provided that such requested NSP amounts are within an agreed range, at a price per liter to be mutually determined. Furthermore, pursuant to the amendment to the 2017 Plasma Purchase Agreement, in the event BPC fails to supply ADMA BioManufacturing with at least a high double digit percentage of ADMA BioManufacturing’s requested NSP amounts, BPC shall promptly reimburse ADMA BioManufacturing the difference in price ADMA BioManufacturing incurs due to BPC’s election not to supply NSP to ADMA BioManufacturing in such amounts as requested. On December 10, 2018, BPC assigned its rights and obligations under the Plasma Purchase Agreement to Grifols, effective January 1, 2019. The Company purchases substantially all of its raw material plasma from Grifols. For the six months ended June 30, 2020, plasma purchases from Grifols totaled approximately $3.7 million, representing approximately 42% of the Company’s total inventory purchases. For the six months ended June 30, 2019, plasma purchases from BPC totaled $5.0 million, or approximately 67% of the Company’s total inventory purchases. Post-marketing commitments In connection with the approval of the BLA for BIVIGAM, on December 19, 2012 Biotest committed to perform two additional post-marketing studies, a pediatric study to evaluate the efficacy and safety of BIVIGAM in children and adolescents, and a post-authorization safety study to further assess the potential risk of hypotension and hepatic and renal impairment in BIVIGAM-treated patients with primary humoral immunodeficiency. These studies are still pending completion, as such ADMA has assumed the remaining obligations, and the costs of the studies will be expensed as incurred as research and development expenses. The Company currently expects both studies to be completed by the end of 2021. In connection with the FDA’s approval of ASCENIV on April 1, 2019, the Company is required to perform a pediatric study to evaluate the safety and efficacy of ASCENIV in children and adolescents. This study is required to be completed by June of 2023. Employment contracts The Company has entered into employment agreements with its executive management team consisting of its President and Chief Executive Officer, its Executive Vice President, Chief Medical Officer and Chief Scientific Officer and its Executive Vice President and Chief Financial Officer. Other commitments In the normal course of business, the Company enters into contracts that contain a variety of indemnifications with its employees, licensors, suppliers and service providers. Further, the Company indemnifies its directors and officers who are, or were, serving at the Company’s request in such capacities. The Company’s maximum exposure under these arrangements is unknown as of June 30, 2020. The Company does not anticipate recognizing any significant losses relating to these arrangements.

SEGMENTS

SEGMENTS	6 Months Ended
	Jun. 30, 2020
SEGMENTS
10. SEGMENTS	10. SEGMENTS The Company is engaged in the manufacture, marketing and development of specialty plasma-derived biologics. The Company’s ADMA BioManufacturing segment reflects the Company’s immunoglobulin manufacturing, commercial and development operations in Boca Raton, FL, acquired on June 6, 2017 (see Note 1).The Plasma Collection Centers segment consists of one FDA-licensed source plasma collection facility, another plasma collection facility for which an FDA license is pending and a plasma collection center currently under construction. The Corporate segment includes general and administrative overhead expenses. The Company defines its segments as those business units whose operating results are regularly reviewed by the chief operating decision maker (“CODM”) to analyze performance and allocate resources. The Company’s CODM is its President and Chief Executive Officer. Summarized financial information concerning reportable segments is shown in the following tables: Three Months Ended June 30, 2020 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 6,502,865 $ 1,249,020 $ 35,709 $ 7,787,594 Cost of product revenue 12,237,141 1,258,488 - 13,495,629 Loss from operations (12,852,835 ) (919,309 ) (3,351,681 ) (17,123,825 ) Interest and other expense, net (235,442 ) (33 ) (2,818,791 ) (3,054,266 ) Net loss (13,088,277 ) (919,342 ) (6,170,472 ) (20,178,091 ) Depreciation and amortization expense 772,241 111,106 2,305 885,652 Total assets 109,105,418 7,542,486 74,893,664 191,541,568 Three Months Ended June 30, 2019 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 4,002,445 $ 2,522,788 $ 35,709 $ 6,560,942 Cost of product revenue 8,170,381 2,320,855 - 10,491,236 Loss from operations (8,671,783 ) (392,181 ) (2,274,710 ) (11,338,674 ) Interest and other expense, net (246,603 ) (59 ) (1,626,536 ) (1,873,198 ) Net loss (8,918,386 ) (392,240 ) (3,901,246 ) (13,211,872 ) Depreciation and amortization expense 688,848 113,958 3,287 806,093 Total assets 67,236,416 3,835,999 72,201,705 143,274,120 Six Months Ended June 30, 2020 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 14,246,139 $ 3,669,782 $ 71,417 $ 17,987,338 Cost of product revenue 26,689,094 3,635,761 - 30,324,855 Loss from operations (25,328,980 ) (1,376,464 ) (7,188,167 ) (33,893,611 ) Interest and other expense, net (474,314 ) (33 ) (5,055,363 ) (5,529,710 ) Net loss (25,803,294 ) (1,376,497 ) (12,243,530 ) (39,423,321 ) Capital expenditures 5,064,494 1,178,790 - 6,243,284 Depreciation and amortization expense 1,447,214 222,395 4,881 1,674,490 Six Months Ended June 30, 2019 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 5,346,428 $ 4,671,686 $ 71,417 $ 10,089,531 Cost of product revenue 16,110,727 3,785,688 - 19,896,415 Loss from operations (19,292,591 ) (362,601 ) (4,891,898 ) (24,547,090 ) Interest and other (expense) income, net (416,216 ) 13,560 (2,895,007 ) (3,297,663 ) Gain on transfer of plasma center assets - 11,527,421 - 11,527,421 Loss on extinguishment of debt - - (9,962,495 ) (9,962,495 ) Net (loss) income (19,708,807 ) 11,178,380 (17,749,400 ) (26,279,827 ) Capital expenditures 224,440 21,235 - 245,675 Depreciation and amortization expense 1,376,240 228,199 6,983 1,611,422

TRANSFER OF PLASMA CENTER ASSET

TRANSFER OF PLASMA CENTER ASSETS	6 Months Ended
	Jun. 30, 2020
TRANSFER OF PLASMA CENTER ASSETS
11. TRANSFER OF PLASMA CENTER ASSETS	11. TRANSFER OF PLASMA CENTER ASSETS As part of the purchase price for the Biotest Transaction (see Note 1), the Company transferred its Marietta, GA and Norcross, GA plasma collection centers to BPC effective January 1, 2019. The Company had estimated the combined fair value of the two facilities to be $12.6 million, and the Company recorded an obligation for this amount as of the date of the Biotest Transaction. On January 1, 2019, upon the transfer of the two plasma collection facilities to BPC, the Company recorded a gain in the amount of $11.5 million, which reflects the derecognition of the obligation to transfer ownership of the two facilities net of the carrying value of the assets associated with these facilities, primarily property and equipment and inventory, in the amount of $1.1 million.

LEASE OBLIGATIONS

LEASE OBLIGATIONS	6 Months Ended
	Jun. 30, 2020
LEASE OBLIGATIONS
12. LEASE OBLIGATIONS	12. LEASE OBLIGATIONS The Company leases certain properties and equipment for its ADMA BioCenters subsidiary and certain equipment for its ADMA BioManufacturing subsidiary, which leases provide the right to use the underlying assets and require lease payments through the respective lease terms which expire at various dates through 2030. The Company’s lease agreements do not contain any material residual value guarantees or material restrictive covenants. The Company determines if an arrangement is an operating lease at inception. Leases with an initial term of 12 months or less are not recorded on the balance sheet. All other leases are recorded on the balance sheet with assets representing the right to use the underlying asset for the lease term and lease liabilities representing the obligation to make lease payments arising from the lease. Right-to-use assets and lease liabilities are recognized at the lease commencement date based on the present value of lease payments over the lease term and include options to extend or terminate the lease when they are reasonably certain to be exercised. The present value of the lease payments is determined using the Company’s incremental borrowing rate of 13%. The Company’s operating lease expense is recognized on a straight-line basis over the lease term and is reflected in Plasma center operating expenses and Selling, general and administrative expenses. Aggregate lease expense and cash paid for the Company’s operating leases for the three months ended June 30, 2020 and 2019 was approximately $0.1 million, and aggregate rent expense and cash paid for the Company’s operating leases for the six months ended June 30, 2020 and 2019 was approximately $0.2 million. In connection with the adoption of ASU 2016-02 on January 1, 2019 (see Note 2), the Company recognized right to use assets of $1.4 million and lease liabilities of approximately $1.6 million. During the six months ended June 30, 2020, the Company entered into two new property leases where the Company has opened or intends to open two new plasma collection facilities. In connection with these leases, the Company recognized aggregate lease liabilities and corresponding right-to-use assets in the approximate amount of $1.7 million. The right-to-use assets are reflected in Deposits and other assets in the accompanying consolidated balance sheets. Including a finance lease the Company entered into in June 2018, the Company has aggregate lease liabilities of $3.1 million and $1.5 million as of June 30, 2020 and December 31, 2019, respectively, which are comprised primarily of the leases for the Company’s plasma collection centers and an administrative office lease in Roswell, GA related to the Company’s ADMA BioCenters subsidiary. The Company’s operating leases have a weighted average remaining term of 8.4 years. Scheduled payments under the Company’s lease obligations are as follows: Remainder of 2020 $ 262,076 Year ended December 31, 2021 699,752 2022 721,005 2023 706,919 2024 603,858 Thereafter 2,205,047 Total payments 5,198,657 Less: imputed interest (2,050,495 ) Current portion (210,870 ) Balance at June 30, 2020 $ 2,937,292 As of July 15, 2020, the Company had entered into two additional property leases where the Company intends to construct additional new plasma collection facilities. The Company has not taken possession of these two leased properties and their lease commencement dates have not been determined. With the exception of advance deposits and initial months’ rent totaling approximately $74,000, no payments have been made under these leases. The initial terms of each lease are from 11 to 13 years with monthly rental payments varying between approximately $17,000 and $21,000, including common area maintenance charges.

SUPPLEMENTAL DISCLOSURE OF CASH

SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION	6 Months Ended
	Jun. 30, 2020
SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION
13. SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION	13. SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION Supplemental cash flow information for the six months ended June 30, 2020 and 2019 is as follows: 2020 2019 SUPPLEMENTAL CASH FLOW INFORMATION: Cash paid for interest $ 4,912,165 $ 3,574,304 Noncash Financing and Investing Activities: Equipment acquired reflected in accounts payable and accrued liabilities $ 1,228,000 $ 290,389 Right-to-use assets obtained in exchange for lease obligations $ 1,723,594 $ 1,421,669 Warrants issued in connection with notes payable $ - $ 3,579,115

SUBSEQUENT EVENTS

SUBSEQUENT EVENTS	6 Months Ended
	Jun. 30, 2020
SUBSEQUENT EVENTS
14. SUBSEQUENT EVENTS	14. SUBSEQUENT EVENTS On August 5, 2020, the Company entered into an Open Market Sale Agreement SM Subject to the terms of the Sale Agreement, the Agent will use its commercially reasonable efforts to sell the Shares from time to time, based upon the Company’s instructions (including any price, time or size limits or other customary parameters or conditions the Company may impose). The Company cannot provide any assurances that it will issue any Shares pursuant to the Sale Agreement. The Company will pay the Agent a commission of up to 3.0% of the gross proceeds from each sale of the Shares under the Sale Agreement. The Company will also reimburse the Agent for certain expenses incurred in connection with the Sale Agreement and agreed to provide the Agent with customary indemnification rights with respect to certain liabilities, including liabilities under the Securities Act and the Securities Exchange Act of 1934, as amended. Through the date of this report, no shares have been sold under the Sale Agreement.

SUMMARY OF SIGNIFICANT ACCOUN_2

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Policies)	6 Months Ended
	Jun. 30, 2020
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Basis of presentation	Basis of presentation The accompanying unaudited condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“U.S. GAAP”) for interim financial information. Any reference in these notes to applicable guidance is meant to refer to U.S. GAAP as found in the Accounting Standards Codification (“ASC”) and Accounting Standards Updates (“ASU”) of the Financial Accounting Standards Board (the “FASB”). The accompanying unaudited condensed consolidated financial statements should be read in conjunction with the annual audited consolidated financial statements and notes thereto as of and for the year ended December 31, 2019 included in the Company’s Annual Report on Form 10-K filed with the U.S. Securities and Exchange Commission (the “SEC”) on March 13, 2020.The accompanying consolidated balance sheet as of December 31, 2019 was derived from the audited financial statements for the year ended December 31, 2019. These condensed consolidated interim financial statements have been prepared in accordance with the instructions to Form 10-Q and Article 8 of Regulation S-X, and therefore omit or condense certain footnotes and other information normally included in complete consolidated financial statements prepared in accordance with U.S. GAAP. All intercompany balances and transactions have been eliminated in consolidation. In the opinion of management, the accompanying unaudited condensed consolidated financial statements include all normal and recurring adjustments (which consist primarily of accruals, estimates and assumptions that impact the financial statements) considered necessary to present fairly the Company’s financial position as of June 30, 2020 and its results of operations, changes in equity and cash flows for the three and six months ended June 30, 2020. During the three and six months ended June 30, 2020 and 2019, comprehensive loss was equal to the net loss amounts presented for the respective periods in the accompanying condensed consolidated statements of operations. Operating results for interim periods are not necessarily indicative of the results that may be expected for the full fiscal year.
Use of estimates	Use of estimates The preparation of financial statements requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates. Significant estimates include the realizable value of accounts receivable, valuation of inventory, assumptions used in projecting future liquidity and capital requirements, assumptions used in the fair value of awards granted under the Company’s equity incentive plans and warrants issued in connection with the issuance of notes payable and the valuation allowance for the Company’s deferred tax assets.
Fair value of financial instruments	Fair value of financial instruments The carrying amounts of certain of the Company’s financial instruments, including cash and cash equivalents, accounts receivable and accounts payable, are shown at cost which approximates fair value due to the short-term nature of these instruments. The debt outstanding under the Company’s senior secured term loan (see Note 6) approximates fair value due to the variable interest rate on this debt. With respect to the subordinated note payable in the amount of $15.0 million as of June 30, 2020 and December 31, 2019 held by Biotest, a principal stockholder of the Company at the time the note was issued concurrent with an acquisition transaction with an affiliate of such stockholder (see Note 6), the Company has concluded that an estimation of fair value for this note is not practicable.
Accounts receivable	Accounts receivable Accounts receivable is reported at realizable value, net of allowances for contractual credits and doubtful accounts, which are recognized in the period the related revenue is recorded. The Company extends credit to its customers based upon an evaluation of each customer's financial condition and credit history. Evaluations of the financial condition and associated credit risk of customers are performed on an ongoing basis. Based on these evaluations, the Company has concluded that its credit risk is minimal. At June 30, 2020, three customers accounted for an aggregate of 76% of the Company’s total accounts receivable, and at December 31, 2019, two customers accounted for 89% of the Company’s total accounts receivable.
Inventories	Inventories Inventories, including plasma intended for resale and plasma intended for internal use in the Company’s manufacturing, commercialization or research and development activities, are carried at the lower of cost or net realizable value determined by the first-in, first-out method. Due to previous uncertainties surrounding certain prior submissions made to the FDA, all costs related to the production of BIVIGAM and ASCENIV prior to their FDA approval dates of May 9, 2019 and April 1, 2019, respectively, have been charged to cost of product revenue in the accompanying consolidated statements of operations during the period the product was produced. In addition, costs associated with the production of conformance or engineering lots that would not qualify as immediately available for commercial sale are charged to cost of product revenue and not capitalized into inventory.
Goodwill	Goodwill Goodwill represents the excess of purchase price over the fair value of net assets acquired by the Company. Goodwill at June 30, 2020 and December 31, 2019 was $3.5 million. All of the Company’s goodwill is attributable to its ADMA BioManufacturing business segment and is related to a 2017acquisition transaction. Goodwill is not amortized, but is assessed for impairment on an annual basis or more frequently if impairment indicators exist. The Company has the option to perform a qualitative assessment of goodwill to determine whether it is more likely than not that the fair value of its reporting unit is less than its carrying amount, including goodwill and other intangible assets. If the Company concludes that this is the case, then it must perform a goodwill impairment test by comparing the fair value of the reporting unit to its carrying value. An impairment charge is recorded to the extent the reporting unit’s carrying value exceeds its fair value, not to exceed the total amount of goodwill allocated to that reporting unit. The Company performs its annual goodwill impairment test as of October 1 of each year. The Company’s annual goodwill impairment test as of October 1, 2019 did not result in a goodwill impairment charge, and the Company did not record any impairment charges related to goodwill for the three and six months ended June 30, 2020 and 2019.
Impairment of long-lived assets	Impairment of long-lived assets The Company assesses the recoverability of its long-lived assets, which include property and equipment and definite-lived intangible assets, whenever significant events or changes in circumstances indicate impairment may have occurred. If indicators of impairment exist, projected future undiscounted cash flows associated with the asset are compared to its carrying amount to determine whether the asset’s carrying value is recoverable. Any resulting impairment is recorded as a reduction in the carrying value of the related asset in excess of fair value and a charge to operating results. For the three and six months ended June 30, 2020 and 2019, the Company determined that there was no impairment of its long-lived assets.
Revenue recognition	Revenue recognition Revenues for the three and six months ended June 30, 2020 and 2019 are comprised of (i) revenues from the sale of the Company’s immunoglobulin products, ASCENIV, BIVIGAM and Nabi-HB, (ii) product revenues from the sale of human plasma collected through the Company’s Plasma Collection Centers business segment, (iii) contract manufacturing revenue, (iv) revenues from the sale of intermediate by-products; and (v) license and other revenues primarily attributable to the out-licensing of ASCENIV to Biotest in 2012 to market and sell this product in Europe and selected countries in North Africa and the Middle East. Biotest has provided the Company with certain services and financial payments in accordance with the related Biotest license agreement and is obligated to pay the Company certain amounts in the future if certain milestones are achieved. Deferred revenue is amortized into income over the term of the Biotest license, representing a period of approximately 22 years. Product revenue is recognized when the customer is deemed to have control over the product. Control is determined based on when the product is shipped or delivered and title passes to the customer. Revenue is recorded in an amount that reflects the consideration the Company expects to receive in exchange. Revenue from the sale of the Company’s immunoglobulin products is recognized when the product reaches the customer’s destination, and is recorded net of estimated rebates, price protection arrangements and customer incentives, including prompt pay discounts, wholesaler chargebacks and other wholesaler fees. These estimates are based on historical experience and certain other assumptions, and the Company believes that such estimates are reasonable. For revenues associated with contract manufacturing and the sale of intermediates, control transfers to the customer and the performance obligation is satisfied when the customer takes possession of the product from the Boca Facility or from a third-party warehouse that is utilized by the Company. Product revenues from the sale of human plasma collected at the Company’s plasma collection centers are recognized at the time control of the product has been transferred to the customer, which generally occurs at the time of shipment. Product revenues are recognized at the time of delivery if the Company retains control of the product during shipment. For the six months ended June 30, 2020, three customers represented an aggregate of 81% of the Company’s consolidated revenues. For the six months ended June 30, 2019, three customers represented an aggregate of 84% of the Company’s consolidated revenues.
Cost of product revenue	Cost of product revenue Cost of product revenue includes costs associated with the manufacture of the Company’s FDA approved products, intermediates and the sale of human source plasma, as well as expenses related to conformance batch production, process development and scientific and technical operations when these operations are attributable to marketed products. When the activities of these operations are attributable to new products in development, the expenses are classified as research and development expenses.
Loss per common share	Loss per common share Basic loss per common share is computed by dividing net loss attributable to common stockholders by the weighted average number of shares of common stock outstanding during the period. Diluted loss per common share is calculated by dividing net loss attributable to common stockholders, as adjusted for the effect of dilutive securities, if any, by the weighted average number of shares of common stock and dilutive common stock outstanding during the period. Potentially dilutive common stock includes the shares of common stock issuable upon the exercise of outstanding stock options and warrants, using the treasury stock method. Potentially dilutive common stock is excluded from the diluted loss per common share computation to the extent that it would be anti-dilutive. As a result, no potentially dilutive securities are included in the computation of any of the accompanying diluted loss per share amounts as the Company reported a net loss for all periods presented. For the six months ended June 30, 2020 and 2019, the following securities were excluded from the calculation of diluted loss per common share because of their anti-dilutive effects: For the Six Months Ended June 30, 2020 2019 Stock options 6,801,779 5,624,603 Restricted stock units 326,000 - Warrants 2,138,160 2,138,160 9,265,939 7,762,763
Stock-based compensation	Stock-based compensation The Company follows recognized accounting guidance which requires all equity-based payments, including grants of stock options, to be recognized in the statement of operations as compensation expense based on their fair values at the date of grant. Compensation expense related to awards to employees and directors with service-based vesting conditions is recognized on a straight-line over the associated vesting period of the award based on the grant date fair value of the award. Stock options granted under the Company’s equity incentive plans generally have a four-year vesting period and a term of 10 years. Pursuant to ASU No. 2016-09, Improvements to Employee Share-Based Payment Accounting (Topic 718)
Income Taxes	Income Taxes The Company recognizes deferred tax assets and liabilities for the expected future tax consequences of events that have been included in the consolidated financial statements or its tax returns. Under this method, deferred tax assets and liabilities are recognized for the temporary differences between the tax bases of assets and liabilities and their respective financial reporting amounts at enacted tax rates in effect for the years in which the temporary differences are expected to reverse. The Company records a valuation allowance on its deferred tax assets if it is more likely than not that the Company will not generate sufficient taxable income to utilize its deferred tax assets. The Company is subject to income tax examinations by major taxing authorities for all tax years since 2015 and for previous periods as it relates to the Company’s net operating loss carryforwards. In accordance with U.S. GAAP, the Company is required to determine whether a tax position of the Company is more likely than not to be sustained upon examination by the applicable taxing authority, including resolution of any related appeals or litigation processes, based on the technical merits of the position. The tax benefit to be recognized is measured as the largest amount of benefit that is greater than fifty percent likely of being realized upon ultimate settlement. Derecognition of a tax benefit previously recognized could result in the Company recording a tax liability that would reduce net assets. Based on its analysis, the Company has determined that it has not incurred any liability for unrecognized tax benefits as of June 30, 2020 and December 31, 2019, and during the three and six months ended June 30, 2020 and 2019, the Company recognized no adjustments for uncertain tax positions.
Recent Accounting Pronouncements	Recent Accounting Pronouncements In June 2016, the FASB issued ASU No. 2016-13, Financial Instruments – Credit Losses (Topic 326) In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842) In July 2017, the FASB issued ASU No. 2017-11, Earnings Per Share (Topic 260), Distinguishing Liabilities from Equity (Topic 480), Derivatives and Hedging (Topic 815)

SUMMARY OF SIGNIFICANT ACCOUN_3

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Tables)	6 Months Ended
	Jun. 30, 2020
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Schedule of dilutive securities	For the Six Months Ended June 30, 2020 2019 Stock options 6,801,779 5,624,603 Restricted stock units 326,000 - Warrants 2,138,160 2,138,160 9,265,939 7,762,763

INVENTORIES (Tables)

INVENTORIES (Tables)	6 Months Ended
	Jun. 30, 2020
INVENTORIES
Schedule of inventory	June 30, December 31, Raw materials $ 24,830,796 $ 33,381,806 Work-in-progress 22,066,417 14,455,665 Finished goods 9,104,135 5,227,263 Total inventories $ 56,001,348 $ 53,064,734

INTANGIBLE ASSETS (Tables)

INTANGIBLE ASSETS (Tables)	6 Months Ended
	Jun. 30, 2020
INTANGIBLE ASSETS
Intangible asset future aggregate amortization expense	Remainder of 2020 $ 357,676 2021 715,352 2022 715,352 2023 715,352 2024 298,065
Schedule of Intangible assets	June 30, 2020 December 31, 2019 Accumulated Accumulated Cost Amortization Net Cost Amortization Net Trademark and other intangible rights related to Nabi-HB $ 4,100,046 $ 1,805,973 $ 2,294,073 $ 4,100,046 $ 1,513,112 $ 2,586,934 Rights to intermediates 907,421 399,697 507,724 907,421 334,881 572,540 Customer contract 1,076,557 1,076,557 - 1,076,557 1,076,557 - $ 6,084,024 $ 3,282,227 $ 2,801,797 $ 6,084,024 $ 2,924,550 $ 3,159,474

PROPERTY AND EQUIPMENT (Tables)

PROPERTY AND EQUIPMENT (Tables)	6 Months Ended
	Jun. 30, 2020
PROPERTY AND EQUIPMENT
Schedule of property and equipment	June 30, 2020 December 31, 2019 Manufacturing and laboratory equipment $ 9,898,186 $ 8,831,817 Office equipment and computer software 2,220,856 1,690,248 Furniture and fixtures 1,400,129 582,088 Construction in process 6,672,211 4,285,915 Leasehold improvements 3,011,009 1,673,084 Land 4,339,441 4,339,441 Buildings and building improvements 16,869,821 16,063,680 44,411,653 37,466,273 Less: Accumulated depreciation (7,038,287 ) (5,724,956 ) Total property and equipment, net $ 37,373,366 $ 31,741,317

DEBT (Tables)

DEBT (Tables)	6 Months Ended
	Jun. 30, 2020
DEBT
Summary of subordinated note payable	June 30, 2020 December 31, 2019 Subordinated note payable to Biotest $ 15,000,000 $ 15,000,000 Less: Debt discount (74,240 ) (91,947 ) Subordinated note payable $ 14,925,760 $ 14,908,053
Summary of notes payable	June 30, 2020 December 31, 2019 Notes payable $ 85,000,000 $ 72,500,000 Less: Debt discount (3,351,813 ) (4,208,837 ) Senior notes payable $ 81,648,187 $ 68,291,163

STOCKHOLDERS' EQUITY (Tables)

STOCKHOLDERS' EQUITY (Tables)	6 Months Ended
	Jun. 30, 2020
STOCKHOLDERS' EQUITY
Schedule of assumptions	Six Months Ended June 30, 2020 2019 Expected term 5.5 - 6.3 years 5.8 - 6.3 years Volatility 62%-67% 54%-62% Dividend yield 0.0 0.0 Risk-free interest rate 0.38-1.68% 1.80-2.92%
Schedule of compensation expense	Shares Weighted Average Grant Date Fair Value Balance at December 31, 2019 - $ - Granted 341,000 $ 2.80 Vested - $ - Forfeited (15,000 ) $ 2.92 Balance at June 30, 2020 326,000 $ 2.80
Schedule of option activity	Shares Weighted Average Exercise Price Balance at December 31, 2019 5,630,351 $ 4.76 Forfeited (47,683 ) $ 3.51 Expired (6,763 ) $ 4.34 Granted 1,232,500 $ 2.96 Exercised (6,626 ) $ 2.03 Balance at June 30, 2020 6,801,779 $ 4.45 Options exercisable 4,030,098 $ 5.19
Schedule of stock-based compensation expense	Three Months Ended June 30, Six Months Ended June 30, 2020 2019 2020 2019 Research and development $ 105,029 $ 89,543 $ 198,603 $ 176,066 Plasma centers 8,510 13,213 15,754 24,753 Selling, general and administrative 539,256 569,349 1,063,145 1,067,820 Cost of product revenue 62,813 54,631 114,654 95,360 Total stock-based compensation expense $ 715,608 $ 726,736 $ 1,392,156 $ 1,363,999

SEGMENTS (Tables)

SEGMENTS (Tables)	6 Months Ended
	Jun. 30, 2020
SEGMENTS
Summarized segment financial information	Three Months Ended June 30, 2020 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 6,502,865 $ 1,249,020 $ 35,709 $ 7,787,594 Cost of product revenue 12,237,141 1,258,488 - 13,495,629 Loss from operations (12,852,835 ) (919,309 ) (3,351,681 ) (17,123,825 ) Interest and other expense, net (235,442 ) (33 ) (2,818,791 ) (3,054,266 ) Net loss (13,088,277 ) (919,342 ) (6,170,472 ) (20,178,091 ) Depreciation and amortization expense 772,241 111,106 2,305 885,652 Total assets 109,105,418 7,542,486 74,893,664 191,541,568 Three Months Ended June 30, 2019 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 4,002,445 $ 2,522,788 $ 35,709 $ 6,560,942 Cost of product revenue 8,170,381 2,320,855 - 10,491,236 Loss from operations (8,671,783 ) (392,181 ) (2,274,710 ) (11,338,674 ) Interest and other expense, net (246,603 ) (59 ) (1,626,536 ) (1,873,198 ) Net loss (8,918,386 ) (392,240 ) (3,901,246 ) (13,211,872 ) Depreciation and amortization expense 688,848 113,958 3,287 806,093 Total assets 67,236,416 3,835,999 72,201,705 143,274,120 Six Months Ended June 30, 2020 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 14,246,139 $ 3,669,782 $ 71,417 $ 17,987,338 Cost of product revenue 26,689,094 3,635,761 - 30,324,855 Loss from operations (25,328,980 ) (1,376,464 ) (7,188,167 ) (33,893,611 ) Interest and other expense, net (474,314 ) (33 ) (5,055,363 ) (5,529,710 ) Net loss (25,803,294 ) (1,376,497 ) (12,243,530 ) (39,423,321 ) Capital expenditures 5,064,494 1,178,790 - 6,243,284 Depreciation and amortization expense 1,447,214 222,395 4,881 1,674,490 Six Months Ended June 30, 2019 ADMA BioManufacturing Plasma Collection Centers Corporate Consolidated Revenues $ 5,346,428 $ 4,671,686 $ 71,417 $ 10,089,531 Cost of product revenue 16,110,727 3,785,688 - 19,896,415 Loss from operations (19,292,591 ) (362,601 ) (4,891,898 ) (24,547,090 ) Interest and other (expense) income, net (416,216 ) 13,560 (2,895,007 ) (3,297,663 ) Gain on transfer of plasma center assets - 11,527,421 - 11,527,421 Loss on extinguishment of debt - - (9,962,495 ) (9,962,495 ) Net (loss) income (19,708,807 ) 11,178,380 (17,749,400 ) (26,279,827 ) Capital expenditures 224,440 21,235 - 245,675 Depreciation and amortization expense 1,376,240 228,199 6,983 1,611,422

LEASE OBLIGATIONS (Tables)

LEASE OBLIGATIONS (Tables)	6 Months Ended
	Jun. 30, 2020
LEASE OBLIGATIONS
Schedule of future minimum lease payments	Remainder of 2020 $ 262,076 Year ended December 31, 2021 699,752 2022 721,005 2023 706,919 2024 603,858 Thereafter 2,205,047 Total payments 5,198,657 Less: imputed interest (2,050,495 ) Current portion (210,870 ) Balance at June 30, 2020 $ 2,937,292

SUPPLEMENTAL DISCLOSURE OF CA_2

SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION (Tables)	6 Months Ended
	Jun. 30, 2020
SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION
Schedule of supplemental cash flow information	2020 2019 SUPPLEMENTAL CASH FLOW INFORMATION: Cash paid for interest $ 4,912,165 $ 3,574,304 Noncash Financing and Investing Activities: Equipment acquired reflected in accounts payable and accrued liabilities $ 1,228,000 $ 290,389 Right-to-use assets obtained in exchange for lease obligations $ 1,723,594 $ 1,421,669 Warrants issued in connection with notes payable $ - $ 3,579,115

ORGANIZATION AND BUSINESS (Deta

ORGANIZATION AND BUSINESS (Details Narrative) - USD ($)	3 Months Ended				6 Months Ended		193 Months Ended
	Jun. 30, 2020	Mar. 31, 2020	Jun. 30, 2019	Mar. 31, 2019	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Dec. 31, 2019	Dec. 31, 2018
ORGANIZATION AND BUSINESS
Cash and cash equivalents	$ 75,781,122		$ 73,615,909		$ 75,781,122	$ 73,615,909	$ 75,781,122	$ 26,752,135	$ 26,754,852
Net loss	(20,178,091)	$ (19,245,230)	$ (13,211,872)	$ (13,067,955)	(39,423,321)	$ (26,279,827)	304,100,000
Working capital	$ 130,100,000				$ 130,100,000		$ 130,100,000

SUMMARY OF SIGNIFICANT ACCOUN_4

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Details) - shares	6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019
Potentially dilutive securities	9,265,939	7,762,763
Stock Options [Member]
Potentially dilutive securities	6,801,779	5,624,603
Restricted stock units [Member]
Potentially dilutive securities	326,000	0
Warrants [Member]
Potentially dilutive securities	2,138,160	2,138,160

SUMMARY OF SIGNIFICANT ACCOUN_5

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Details Narrative) - USD ($)	6 Months Ended		12 Months Ended
	Jun. 30, 2020	Jun. 30, 2019	Dec. 31, 2019
Goodwill	$ 3,529,509		$ 3,529,509
Vesting term	10 years
Right of use assets	$ 1,700,000
Lease liability	$ 3,100,000		$ 1,500,000
Customer Three [Member]
Risk concentration	8100.00%	8400.00%
Customer Three [Member] | Accounts Receivable [Member]
Risk concentration	7600.00%
Customer Two [Member] | Accounts Receivable [Member]
Risk concentration			8900.00%
Biotest [Member]
Note payable	$ 15,000,000		$ 15
January 1, 2019 [Member]
Right of use assets	1,400,000
Lease liability	$ 1,600,000

INVENTORIES (Details)

INVENTORIES (Details) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
INVENTORIES
Raw materials	$ 24,830,796	$ 33,381,806
Work-in-process	22,066,417	14,455,665
Finished goods	9,104,135	5,227,263
Total inventories	$ 56,001,348	$ 53,064,734

INTANGIBLE ASSETS (Details)

INTANGIBLE ASSETS (Details) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
Cost	$ 6,084,024	$ 6,084,024
Accumulated amortization	3,282,227	2,924,550
Net	2,801,797	3,159,474
Trademark and other intangible rights related to Nabi-HB [Member]
Cost	4,100,046	4,100,046
Accumulated amortization	1,805,973	1,513,112
Net	2,294,073	2,586,934
Right to intermediates [Member]
Cost	907,421	907,421
Accumulated amortization	399,697	334,881
Net	507,724	572,540
Customer contract [Member]
Cost	1,076,557	1,076,557
Accumulated amortization	1,076,557	1,076,557
Net	$ 0	$ 0

INTANGIBLE ASSETS (Details 1)

INTANGIBLE ASSETS (Details 1)	Jun. 30, 2020USD ($)
INTANGIBLE ASSETS
Remainder of 2020	$ 357,676
2021	715,352
2022	715,352
2023	715,352
2024	$ 298,065

INTANGIBLE ASSETS (Details Narr

INTANGIBLE ASSETS (Details Narrative) - USD ($)	3 Months Ended		6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
INTANGIBLE ASSETS
Amortization expense	$ 200,000	$ 0.2	$ 400,000	$ 0.4

PROPERTY AND EQUIPMENT (Details

PROPERTY AND EQUIPMENT (Details) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
Property, plant and equipment, gross	$ 44,411,653	$ 37,466,273
Less: accumulated depreciation and amortization	(7,038,287)	(5,724,956)
Property, plant and equipment, net	37,373,366	31,741,317
Manufacturing and laboratory equipment [Member]
Property, plant and equipment, gross	9,898,186	8,831,817
Office equipment and computer software [Member]
Property, plant and equipment, gross	2,220,856	1,690,248
Furniture and fixtures [member]
Property, plant and equipment, gross	1,400,129	582,088
Leasehold improvements [Member]
Property, plant and equipment, gross	3,011,009	1,673,084
Land [Member]
Property, plant and equipment, gross	4,339,441	4,339,441
Buildings [Member]
Property, plant and equipment, gross	16,869,821	16,063,680
Construction in process [Member]
Property, plant and equipment, gross	$ 6,672,211	$ 4,285,915

PROPERTY AND EQUIPMENT (Detai_2

PROPERTY AND EQUIPMENT (Details Narrative) - USD ($) $ in Millions	3 Months Ended		6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
Depreciation expense	$ 0.7	$ 0.6	$ 1.3	$ 1.2
Buildings [Member]
Useful life			30 years
Property and equipment [Member] | Maximum [Member]
Useful life			10 years

DEBT (Details)

DEBT (Details) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
DEBT
Notes payable	$ 85,000,000	$ 72,500,000
Less:
Debt discount	(3,351,813)	(4,208,837)
Senior notes payable	$ 81,648,187	$ 68,291,163

DEBT (Details 1)

DEBT (Details 1) - USD ($)	Jun. 30, 2020	Dec. 31, 2019
DEBT
Subordinated note payable to Biotest	$ 15,000,000	$ 15,000,000
Less:
Debt discount	(74,240)	(91,947)
Subordinated note payable	$ 14,925,760	$ 14,908,053

DEBT (Details Narrative)

DEBT (Details Narrative) - USD ($)	Feb. 11, 2019	May 03, 2019	May 02, 2019	Jun. 30, 2020	Mar. 31, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
Perceptive Tranche I Note and Perceptive Tranche II fees paid		$ 5,300,000					$ 30,000,000
Interest rate		141.00%
Description of prepaid principal amount							(i) 5.0% of the prepaid principal amount, if prepaid on or prior to the first anniversary of the Perceptive Closing Date, (ii) 4.0% of the prepaid principal amount, if prepaid after the first anniversary of the Perceptive Closing Date and on or prior to the second anniversary of the Perceptive Closing Date, or (iii) 3.0% of the prepaid principal amount, if prepaid after the second anniversary of the Perceptive Closing Date and on or prior to the third anniversary of the Perceptive Closing Date.
Warrant, amount				$ 6,255	$ 7,177	$ 75,048
Warrant exercise price							$ 2.96
Loss on the extinguishment of debt				$ 0		$ 0	$ 0	$ 9,962,495
Perceptive Tranche III Warrant [Member]
Warrant			250,000
Warrant, amount			$ 900,000
Warrant exercise price			$ 4.64
Perceptive Tranche III Loan (Member)
Principal amount of term loan		$ 12,500,000
Perceptive Tranche II Loan (Member)
Principal amount of term loan		27,500,000
Perceptive Tranche I Loan (Member)
Principal amount of term loan							$ 45,000,000
BPC (Member)
Interest rate							60.00%
Expiration date							June 6, 2022
Net Cash proceeds							$ 15,000,000
Marathon Healthcare Finance Fund, L.P. (Member)
Deferred facility fee		2,800,000
Loss on the extinguishment of debt								(9,962,495)
Prepayment Penalty		6,500,000						6,500,000
Unamortized debt discount								$ 3,500,000
Fees and expenses		1,500,000
Additional facility fee		100,000
Debt service reserve		4,000,000
Accrued interest		$ 700,000
Perceptive Credit Agreement [Member]
Principal amount of term loan	$ 85,000,000
Additionlal description							In addition, the Company must (i) at all times prior to the Maturity Date maintain a minimum cash balance of $3.0 million; and (ii) as of the last day of each fiscal quarter commencing with the fiscal quarter ended June 30, 2019, report revenues for the trailing 12-month period that exceed the amounts set forth in the Perceptive Credit Agreement, which range from $7.0 million for the fiscal quarter ended June 30, 2019 to $55.0 million for the fiscal quarter ending December 31, 2021.
Interest rate description							Perceptive Credit Agreement bear interest at a rate per annum equal to 7.5% plus the greater of (i) one-month LIBOR and (ii) 3.5%; provided, however, that upon, and during the continuance of, an Event of Default, the interest rate will automatically increase by an additional 400 basis points. Accrued interest is payable to Perceptive on the last day of each month during the term of the Perceptive Credit Facility.The rate of interest in effect as of the Perceptive Closing Date and at June 30, 2020 was 11.0%.
Warrant							1,360,000
Warrant, amount							$ 2,700,000
Expiration date							February 11, 2029
Warrant exercise price							$ 3.28

STOCKHOLDERS EQUITY (Details)

STOCKHOLDERS EQUITY (Details)	6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019
Dividend yield	0.00%	0.00%
Maximum [Member]
Expected term	6 years 3 months 18 days	6 years 3 months 18 days
Volatility	6700.00%	6200.00%
Risk-free interest rate	1.68%	2.92%
Minimum [Member]
Expected term	5 years 6 months	5 years 9 months 18 days
Volatility	6200.00%	5400.00%
Risk-free interest rate	0.38%	1.80%

STOCKHOLDERS EQUITY (Details 1)

STOCKHOLDERS EQUITY (Details 1)	6 Months Ended
	Jun. 30, 2020$ / sharesshares
Shares
Outstanding at beginning of period | shares	5,630,351
Forfeited | shares	(47,683)
Expired | shares	(6,763)
Granted | shares	1,232,500
Exercised | shares	(6,626)
Outstanding at end of period | shares	6,801,779
Options exercisable | shares	4,030,098
Weighted Average Exercise Price
Outstanding at beginning of period | $ / shares	$ 4.76
Forfeited | $ / shares	3.51
Expired | $ / shares	4.34
Granted | $ / shares	2.96
Exercised | $ / shares	2.03
Outstanding at end of period | $ / shares	4.45
Options exercisable | $ / shares	$ 5.19

STOCKHOLDERS EQUITY (Details 2)

STOCKHOLDERS EQUITY (Details 2)	6 Months Ended
	Jun. 30, 2020$ / sharesshares
Shares
Outstanding at beginning of period | shares	5,630,351
Granted | shares	1,232,500
Forfeited | shares	(47,683)
Outstanding at end of period | shares	6,801,779
Weighted Average Exercise Price
Outstanding at beginning of period | $ / shares	$ 4.76
Granted | $ / shares	2.96
Forfeited | $ / shares	3.51
Outstanding at end of period | $ / shares	$ 4.45
Restricted stock units [Member]
Shares
Outstanding at beginning of period | shares	0
Granted | shares	341,000
Vested | shares	0
Forfeited | shares	(15,000)
Outstanding at end of period | shares	326,000
Weighted Average Exercise Price
Outstanding at beginning of period | $ / shares	$ 0
Granted | $ / shares	2.80
Vested | $ / shares	0
Forfeited | $ / shares	2.92
Outstanding at end of period | $ / shares	$ 2.80

STOCKHOLDERS EQUITY (Details 3)

STOCKHOLDERS EQUITY (Details 3) - USD ($)	3 Months Ended		6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
Stock-based compensation	$ 715,608	$ 726,736	$ 1,392,156	$ 1,363,999
Research and development [Member]
Stock-based compensation	105,029	89,543	15,754	176,066
Plasma centers [Member]
Stock-based compensation	8,510	13,213	15,754	24,753
Selling, general and administrative [Member]
Stock-based compensation	539,256	569,349	1,063,145	1,067,820
Cost of product revenue [Member]
Stock-based compensation	$ 62,813	$ 54,631	$ 114,654	$ 95,360

STOCKHOLDERS EQUITY (Details Na

STOCKHOLDERS EQUITY (Details Narrative) - USD ($)	Feb. 11, 2020	Feb. 21, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019	Dec. 31, 2019
Preferred stock, par value				$ 0.0001		$ 0.0001
Preferred stock, shares authorized				10,000,000		10,000,000
Preferred stock, outstanding				0		0
Common stock, par value				$ 0.0001		$ 0.0001
Common stock, shares authorized				150,000,000		150,000,000
Underwritten public offering	23,500,000	3,525,000
Common stock shares, issued				86,349,981		59,318,355
Gross proceeds from public offering	$ 82,300,000	$ 12,300,000		$ 88,700,000
Common stock, outstanding				86,349,981		59,318,355
Common stock reserved for outstanding				9,265,939
Common stock issuable				54,384,080
Warrants outstanding				2,138,160		2,138,160
Weighted average exercise price of warrants				$ 3.81
Restricted stock units [Member]
Unrecognized compensation expense recognition period				3 years 6 months
Unrecognized compensation expense				$ 800,000
Compensation expense			$ 0.1	$ 100,000
Common stock granted				341,000
Equity Incentive Plans [Member]
Unrecognized compensation expense recognition period				2 years 7 months 6 days
Options granted				1,232,500	1,429,100
Weighted average remaining contractual life of stock options exercisable				5 years 7 months 6 days
Weighted average remaining contractual life of stock options outstanding				6 years 10 months 24 days
Unrecognized compensation expense				$ 5,100,000

RELATED PARTY TRANSACTIONS (Det

RELATED PARTY TRANSACTIONS (Details Narrative) - USD ($)	1 Months Ended	3 Months Ended		6 Months Ended
	Oct. 01, 2017	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019
Credit facility				1000.00%
Public offering description				(i) Perceptive Advisors, a principal stockholder of ADMA, purchased 4,563,700 shares of common stock through one of its affiliates, (ii) Dr. Grossman purchased 22,857 shares of common stock directly and 22,857 shares indirectly through an entity he controls (iii) Lawrence P. Guiheen, a director of the Company, purchased 20,000 shares of common stock, (iv) Mr. Grossman purchased 28,571 shares of common stock directly and 57,143 shares indirectly through an entity he controls (v) Brian Lenz, the Company’s Executive Vice President and Chief Financial Officer, purchased 7,142 shares of common stock, and (vi) James Mond, the Company’s Chief Scientific Officer and Chief Medical Officer, purchased 4,285 shares of common stock, all at the public offering price of $3.50 per share.
Rent expense		$ 100,000	$ 0.1	$ 200,000	$ 0.2
Areth, LLC [Member]
Rent expense				$ 60,000	$ 60,000
Monthly Rent	$ 10,000
Debt instrument, frequency of periodic payment	monthly

COMMITMENTS AND CONTINGENCIES (

COMMITMENTS AND CONTINGENCIES (Details Narrative) - USD ($) $ in Millions	6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019
COMMITMENT AND CONTINGENCIES
Purchase percentage from inventory	4200.00%	6700.00%
Purchase of raw material	$ 3.7	$ 5
Plasma supply agreement term	10 years

SEGMENTS (Details)

SEGMENTS (Details) - USD ($)	3 Months Ended				6 Months Ended		193 Months Ended
	Jun. 30, 2020	Mar. 31, 2020	Jun. 30, 2019	Mar. 31, 2019	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020
Revenues	$ 7,787,594		$ 6,560,942		$ 17,987,338	$ 10,089,531
Cost of product revenue	13,495,629		10,491,236		30,324,855	19,896,415
Loss from operations	(17,123,825)		(11,338,674)		(33,893,611)	(24,547,090)
Gain on transfer of plasma center assets	0		0		0	11,527,421
Loss on the extinguishment of debt	0		0		0	9,962,495
Net loss	(20,178,091)	$ (19,245,230)	(13,211,872)	$ (13,067,955)	(39,423,321)	(26,279,827)	$ 304,100,000
Depreciation and amortization expense					1,674,490	1,611,422
Consolidated (member)
Revenues	7,787,594		6,560,942		17,987,338	10,089,531
Cost of product revenue	13,495,629		10,491,236		30,324,855	19,896,415
Loss from operations	(17,123,825)		(11,338,674)		(33,893,611)	(24,547,090)
Interest and other expense, net	(3,054,266)		(1,873,198)		(5,529,710)	(3,297,663)
Gain on transfer of plasma center assets	0					11,527,421
Loss on the extinguishment of debt						(9,962,495)
Net loss	(20,178,091)		(13,211,872)		(39,423,321)	(26,279,827)
Capital expenditure	6,243,284				6,243,284	245,675
Depreciation and amortization expense	885,652		806,093		1,674,490	1,611,422
TOTAL ASSETS	191,541,568		143,274,120
Plasma Collection Centers
Revenues	1,249,020		2,522,788		3,669,782	4,671,686
Cost of product revenue	1,258,488		2,320,855		3,635,761	3,785,688
Loss from operations	(919,309)		(392,181)		(1,376,464)	(362,601)
Interest and other expense, net	(33)		(59)		(33)	13,560
Gain on transfer of plasma center assets	0		0			11,527,421
Loss on the extinguishment of debt	0		0
Net loss	(919,342)		(392,240)		(1,376,497)	11,178,380
Capital expenditure					1,178,790	21,235
Depreciation and amortization expense	111,106		113,958		222,395	228,199
TOTAL ASSETS	7,542,486		3,835,999
Corporate
Revenues	35,709		35,709		71,417	71,417
Cost of product revenue	0		0
Loss from operations	(3,351,681)		(2,274,710)		(7,188,167)	(4,891,898)
Interest and other expense, net	(2,818,791)		(1,626,536)		(5,055,363)	(2,895,007)
Gain on transfer of plasma center assets	0		0
Loss on the extinguishment of debt						(9,962,495)
Net loss	(6,170,472)		(3,901,246)		(12,243,530)	(17,749,400)
Capital expenditure	0		0		6,243,284	245,675
Depreciation and amortization expense	2,305		3,287		4,881	6,983
TOTAL ASSETS	74,893,664		72,201,705
ADMA BioManufacturing
Revenues	6,502,865		4,002,445		14,246,139	5,346,428
Cost of product revenue	12,237,141		8,170,381		26,689,094	16,110,727
Loss from operations	(12,852,835)		(8,671,783)		(25,328,980)	(19,292,591)
Interest and other expense, net	(235,442)		(246,603)		(474,314)	(416,216)
Gain on transfer of plasma center assets	0		0
Net loss	(13,088,277)		(8,918,386)		(25,803,294)	(19,708,807)
Capital expenditure					5,064,494	224,440
Depreciation and amortization expense	772,241		688,848		$ 1,447,214	$ 1,376,240
TOTAL ASSETS	$ 109,105,418		$ 67,236,416

TRANSFER OF PLASMA CENTER ASS_2

TRANSFER OF PLASMA CENTER ASSETS (Details Narrative) - USD ($) $ in Millions	Jun. 30, 2020	Jan. 01, 2019
TRANSFER OF PLASMA CENTER ASSETS
Gain upon transfer facilities		$ 11.5
Net carrying value of assets		$ 1.1
Combined fair value of obligation	$ 12.6

LEASE OBLIGATIONS (Details)

LEASE OBLIGATIONS (Details)	Jun. 30, 2020USD ($)
LEASE OBLIGATIONS
Remainder of 2020	$ 262,076
2021	699,752
2022	721,005
2023	706,919
2024	603,858
Thereafter	2,205,047
Total payments	5,198,657
Less: imputed interest	2,050,495
Current portion	210,870
Total	$ 2,937,292

LEASE OBLIGATIONS (Details Narr

LEASE OBLIGATIONS (Details Narrative) - USD ($)	Jul. 15, 2020	Jun. 30, 2020	Jun. 30, 2019	Jun. 30, 2020	Jun. 30, 2019	Dec. 31, 2019
Lease and rent expense		$ 100,000	$ 0.1	$ 200,000	$ 0.2
Lease description	With the exception of advance deposits and initial months’ rent totaling approximately $74,000, no payments have been made under these leases. The initial terms of each lease are from 11 to 13 years with monthly rental payments varying between approximately $17,000 and $21,000, including common area maintenance charges.
Operating Lease liabilities		$ 3,100,000		$ 3,100,000		$ 1,500,000
Weighted average remaining term		8 years 4 months 24 days		8 years 4 months 24 days
Right of use asstes		$ 1,700,000		$ 1,700,000
Incremental borrowing rate				1300.00%
January 1, 2019 [Member]
Operating Lease liabilities		1,600,000		$ 1,600,000
Right of use asstes		$ 1,400,000		$ 1,400,000

SUPPLEMENTAL DISCLOSURE OF CA_3

SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION (Details) - USD ($)	6 Months Ended
	Jun. 30, 2020	Jun. 30, 2019
SUPPLEMENTAL INFORMATION:
Cash paid for interest	$ 4,912,165	$ 3,574,304
Noncash Financing and Inesting Activities:
Equipment acquired reflected in accounts payable and accrued liabilities	1,228,000	290,389
Right-to-use assets obtained in exchange for lease obligations	1,723,594	1,421,669
Warrants issued in connection with note payable	$ 0	$ 3,579,115

SUBSEQUENT EVENTS (Details Narr

SUBSEQUENT EVENTS (Details Narrative) - $ / shares	6 Months Ended
	Jun. 30, 2020	Dec. 31, 2019
Common stock, par value	$ 0.0001	$ 0.0001
Subsequent Event [Member] | Sale Agreement [Member] | Jefferies LLC [Member]
Common stock, par value	$ 0.0001
Subsequent Event [Member] | Sale Agreement [Member] | Jefferies LLC [Member] | Maximum [Member]
Common stock offering	50,000,000
Commission description	The Company will pay the Agent a commission of up to 3.0% of the gross proceeds from each sale of the Shares under the Sale Agreement.