Quarterly
net revenues of
$266.0
million, an increase of
25.9%
year-over-year
Purified Cortrophin
®
Gel net revenues of
$117.1
million, an increase of
43.5%
year-over-year
Quarterly GAAP net income available to common shareholders of
$24.7
million; Quarterly adjusted non-GAAP EBITDA of
$71.6
million, an increase of
32.4%
year-over-year
Diluted GAAP income per share of
$1.05
and adjusted non-GAAP diluted earnings per share of
$2.21
Reaffirming 2026 guidance for total net revenue of
$1,080
-
$1,140
million and adjusted non-GAAP EBITDA of
$285
-
$300
million
PRINCETON, N.J., Aug. 07, 2026 (GLOBE NEWSWIRE) -- ANI Pharmaceuticals, Inc. (Nasdaq: ANIP) (ANI or the Company) today announced financial results and business highlights for the second quarter ended June 30, 2026.
“In the second quarter, we delivered outstanding financial results, while we implemented the largest Rare Disease sales force expansion in our history,” said Nikhil Lalwani, President and CEO of ANI. “Leading indicators from our gout expansion for Cortrophin Gel are very positive, with the team rapidly delivering a large funnel of new patient cases, with significant breadth and depth of prescribing. The encouraging initial trends we are seeing from the gout expansion, and the continued momentum in our existing specialties, further support our conviction in Cortrophin Gel’s sizable multi-year growth opportunity.”
“We are reaffirming our full year 2026 total net revenue guidance of $1,080 - $1,140 million and adjusted non-GAAP EBITDA of $285 - $300 million. Based on our results in the first half of 2026, we are modestly adjusting our Cortrophin Gel net revenue guidance to $520 - $540 million, reflecting 50-55% growth for the full year. Our solid track record of commercial execution and prudent capital allocation combined with our strong balance sheet position us well for continued shareholder value creation,” he concluded.
Second Quarter and Recent Business Highlights:
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Rare Disease
Cortrophin Gel:
Cortrophin Gel net revenues were $117.1 million for the second quarter of 2026, an increase of 43.5% over the same period in 2025. Year-over-year growth in the second quarter of 2026 was driven primarily by the existing specialty areas of Nephrology, Neurology, Ophthalmology, Pulmonology and Rheumatology. Momentum for the existing specialties has continued into the third quarter with a record number of new cases initiated in July.
ANI’s organization expansion to reach podiatrists and primary care physicians for Cortrophin Gel in acute gouty arthritis flares was fully operational as of the end of June, as planned.
The Company’s key demand metrics of the gout expansion have been very positive to date, with over 95% of the reps generating multiple new patient cases and over a third of the prescribers initiating two or more cases, and the Company has seen balanced demand from both podiatrists and primary care physicians.
The gout expansion targets an estimated addressable market of approximately 285,000 patients, the majority of whom are treated by podiatrists and primary care physicians.
ILUVIEN:
ILUVIEN
®
net revenues were $18.7 million for the second quarter of 2026, a decrease of 16.1% over the same period in 2025 based primarily on timing of international shipments.
The Company announced 6-month topline data from the Phase 4 open-label single-arm SYNCHRONICITY clinical trial in chronic non-infectious uveitis affecting the posterior segment of the eye (NIU-PS) and anticipates announcing the detailed results and additional analyses at a key medical conference attended by retina specialists in the fourth quarter of 2026.
Generics
Generics net revenues were $99.1 million in the second quarter of 2026, an increase of 9.7% over the same period in 2025, driven by new product launches, including the partnered generic launch that commenced in the third quarter of 2025.
Launched 12 new Generics products year-to-date, and on track for at least 15 new product launches in 2026.
Brand Royalties and Other Revenues
The Company recognized $17.7 million of revenue under the Harmony Agreement, comprised of $9.7 million of royalties on net sales of pitolisant-based products for the second quarter of 2026, and $8.0 million based upon work completed in the quarter toward the achievement of certain development milestones. The balance of the development work is expected to be completed in the third quarter of 2026, at which time the Company will recognize an additional $2.0 million in development milestone revenue. In addition, the Company will continue to earn low single digit royalties on net sales of pitolisant-based products.
Brands
Brands net revenues were $11.8 million for the second quarter of 2026, a decrease of 10.5% over the same period in 2025, reflecting a normalization in demand for certain products.
Corporate Highlights
Effective on May 8, 2026, ANI’s board of directors authorized a share repurchase program to repurchase up to $100.0 million in common stock through May 2029.
Second Quarter 2026 Financial Results
Three Months Ended June 30,
(in thousands)
2026
2025
Change
% Change
Rare Disease and Brands
Cortrophin Gel
$
117,126
$
81,647
$
35,479
43.5
%
ILUVIEN and YUTIQ
(1)
18,718
22,316
(3,598
)
(16.1
)%
Rare Disease total net revenues
$
135,844
$
103,963
$
31,881
30.7
%
Brands
11,813
13,195
(1,382
)
(10.5
)%
Brand royalties and other revenues
17,731
—
17,731
100.0
%
Rare Disease and Brands total net revenues
$
165,388
$
117,158
$
48,230
41.2
%
Generics and Other
Generic pharmaceutical products
99,051
90,297
8,754
9.7
%
Other generic revenues
1,605
3,916
(2,311
)
(59.0
)%
Generics and Other total net revenues
$
100,656
$
94,213
$
6,443
6.8
%
Total net revenues
$
266,044
$
211,371
$
54,673
25.9
%
(1)
There were no sales of YUTIQ during the quarter ended June 30, 2026, as the Company transitioned promotional efforts in the U.S. from YUTIQ to ILUVIEN, which has a combined label of DME and NIU-PS during the second quarter of 2025.
All comparisons are made versus the same period in 2025 unless otherwise stated.
Total net revenues for the second quarter of 2026 were $266.0 million, an increase of 25.9% over the prior year period.
Net revenues for Rare Disease, which includes Cortrophin Gel and ILUVIEN, increased 30.7% to $135.8 million. Cortrophin Gel net revenues increased 43.5% to $117.1 million and ILUVIEN net revenues decreased 16.1% to $18.7 million. Growth for Cortrophin was driven primarily by increased volume while ILUVIEN was impacted by timing of shipments in certain international markets.
Net revenues for Brands decreased 10.5% to $11.8 million driven by normalization in demand for certain products.
Net revenues from Brand royalties and other revenues include $8.0 million of revenue recognized upon work completed in the quarter toward the achievement of certain development milestones and royalties of approximately $9.7 million, related to the Harmony Agreement.
Net revenues for Generic pharmaceutical products increased 9.7% to $99.1 million driven by continued strength in the partnered generic launch that commenced in the third quarter of 2025, contribution from new product launches and commercial and operational outperformance.
On a GAAP basis, gross margin decreased from 64.7% to 62.4%, while on a non-GAAP basis, gross margin decreased from 64.9% to 62.6%. Both decreases were primarily due to higher sales of royalty bearing products, including Cortrophin Gel and a partnered generic product that launched in the third quarter of 2025, and the non-recurrence of prior year revenues from Prucalopride. These effects were somewhat tempered by the revenue recognized under the Harmony Agreement.
On a GAAP basis and a non-GAAP basis, research and development expenses decreased 10.8% to $14.7 million and 11.4% to $14.1 million, respectively, driven by timing associated with ongoing and new projects to support future growth of our Rare Disease and Generics businesses.
On a GAAP basis, selling, general, and administrative expenses increased 12.1% to $91.7 million, while on a non-GAAP basis, selling, general, and administrative expenses increased 20.2% to $80.7 million. Both comparisons include incremental expense related to the initial marketing and recruitment expense of our expansion of the Rare Disease team, which is targeting opportunities in acute gouty arthritis, and an overall increase in activities to support the growth of our business.
On a GAAP basis, the Company reported net income attributable to common shareholders of $24.7 million, or $1.05 per diluted share, for the second quarter of 2026 compared to $8.1 million, or $0.36 per diluted share, in the prior year period. On a non-GAAP basis, the Company reported adjusted diluted earnings per share of $2.21 for the second quarter of 2026 compared to $1.80 in the prior year period.
Adjusted non-GAAP EBITDA for the second quarter of 2026 was $71.6 million, an increase of 32.4% from the second quarter of 2025, driven by increased net revenues and gross profit.
For reconciliations of adjusted non-GAAP metrics, including non-GAAP gross margin, non-GAAP research and development expenses, non-GAAP selling, general and administrative expenses, adjusted non-GAAP EBITDA and adjusted non-GAAP diluted earnings per share to the most directly comparable GAAP financial measures, please see Table 3, Table 4, and Table 5 below, respectively.
Liquidity
As of June 30, 2026, the Company had $360.2 million in unrestricted cash and cash equivalents, $274.5 million in net accounts receivable and $620.9 million in principal value of outstanding debt (inclusive of the Company’s senior convertible notes). The Company generated cash flow from operations of $115.0 million on a year to date basis.
Full Year 2026 Financial Guidance
Revised Full Year 2026
Guidance
Previous Full Year 2026 Guidance
2025 Actual
Growth
Net Revenue (Total Company)
$1,080 million - $1,140 million
$1,080 million - $1,140 million
$883 million
22% - 29%
Cortrophin Gel Net Revenue
$520 million - $540 million
$540 million - $575 million
$348 million
50% - 55%
ILUVIEN Net Revenue
$78 million - $83 million
$78 million - $83 million
$75 million
4% - 11%
Adjusted Non-GAAP EBITDA
$285 million - $300 million
$285 million - $300 million
$230 million
24% - 31%
Adjusted Non-GAAP Diluted EPS
$9.19 - $9.69
$9.19 - $9.69
$7.89
16% - 23%
ANI expects full year total company adjusted non-GAAP gross margin between 59.9% and 60.9% and anticipates approximately 21.5 million and 21.8 million shares outstanding for the purpose of calculating full year adjusted non-GAAP diluted EPS. The Company expects its annual U.S. GAAP effective tax rate to be between 26% and 28% and will continue to tax effect non-GAAP adjustments for computation of adjusted non-GAAP diluted earnings per share utilizing a tax rate of 26%.
Conference Call
The Company’s management will host a conference call and webcast today, Friday, August 7, at 8:00 a.m. ET to discuss its second quarter 2026 results.
To view the webcast, please click
here
. Links to access the webcast and conference call will also be available on the “Events & Presentations” page of the Company’s website at
, under the “Investors” section. A replay of the event will remain accessible for up to one year.
Non-GAAP Financial Measures
Adjusted non-GAAP EBITDA
ANI’s management considers adjusted non-GAAP EBITDA to be an important financial indicator of ANI’s operating performance, providing investors and analysts with a useful measure of operating results unaffected by non-cash stock-based compensation and differences in capital structures, tax structures, capital investment cycles, ages of related assets, and compensation structures among otherwise comparable companies. Management uses adjusted non-GAAP EBITDA when analyzing Company performance.
Adjusted non-GAAP EBITDA is defined as net income, excluding tax expense, interest expense, net, other expense (income), net, depreciation and amortization expense, non-cash stock-based compensation expense, M&A transaction and integration expenses, contingent consideration fair value adjustments, unrealized gain (loss) on our investment in equity securities, expenses incurred and settlement payments received in connection with certain litigation matters, severance expenses, and certain other items that vary in frequency and impact on ANI’s results of operations. Adjusted non-GAAP EBITDA should be considered in addition to, but not in lieu of, net income or loss reported under GAAP. A reconciliation of adjusted non-GAAP EBITDA to the most directly comparable GAAP financial measure is provided below.
ANI is not providing a reconciliation for the forward-looking full year 2026 adjusted EBITDA guidance because it does not currently have sufficient information to accurately estimate all of the variables and individual adjustments for such reconciliation, including “with” and “without” tax provision information. As such, ANI’s management cannot estimate on a forward-looking basis without unreasonable effort the impact these variables and individual adjustments will have on its reported results.
Adjusted non-GAAP Net Income
ANI’s management considers adjusted non-GAAP net income to be an important financial indicator of ANI’s operating performance, providing investors and analysts with a useful measure of operating results unaffected by the non-cash stock-based compensation, non-cash interest expense, depreciation and amortization, M&A transaction and integration expenses, contingent consideration fair value adjustment, unrealized (gain) loss on our investment in equity securities, expenses incurred and settlement payments received in connection with certain litigation matters, severance expense, and certain other items that vary in frequency and impact on ANI’s results of operations. Management uses adjusted non-GAAP net income when analyzing Company performance.
Adjusted non-GAAP net income is defined as net income, plus the non-cash stock-based compensation, non-cash interest expense, depreciation and amortization, M&A transaction and integration expenses, contingent consideration fair value adjustment, unrealized (gain) loss on our investment in equity securities, expenses incurred and settlement payments received in connection with certain litigation matters, severance expense, and certain other items that vary in frequency and impact on ANI’s results of operations, less the tax impact of these adjustments calculated using an estimated statutory tax rate. Management will continually analyze this metric and may include additional adjustments in the calculation in order to provide further understanding of ANI’s results. Adjusted non-GAAP net income should be considered in addition to, but not in lieu of, net income reported under GAAP. A reconciliation of adjusted non-GAAP net income to the most directly comparable GAAP financial measure is provided below.
Adjusted non-GAAP Diluted Earnings per Share
ANI’s management considers adjusted non-GAAP diluted earnings per share to be an important financial indicator of ANI’s operating performance, providing investors and analysts with a useful measure of operating results unaffected by the non-cash stock-based compensation, non-cash interest expense, depreciation and amortization, M&A transaction and integration expenses, contingent consideration fair value adjustment, unrealized (gain) loss on our investment in equity securities, expenses incurred and settlement payments received in connection with certain litigation matters, severance expense, and certain other items that vary in frequency and impact on ANI’s results of operations. Management uses adjusted non-GAAP diluted earnings per share when analyzing Company performance.
Non-GAAP Adjusted Diluted Weighted-Average Shares Outstanding exclude certain dilutive shares related to the senior convertible notes as they are intended to be covered by our capped call transactions. Our outstanding capped call transactions are intended to fully offset the dilutive effect of the senior convertible notes recognized in the calculation of GAAP diluted EPS, and therefore 340,000 shares and 345,000 shares, for the three and six months ended June 30, 2026, respectively, have been excluded from the calculation of Non-GAAP Adjusted Diluted Weighted-Average Shares Outstanding.
Adjusted non-GAAP diluted earnings per share is defined as adjusted non-GAAP net income, as defined above, divided by the diluted weighted average shares outstanding during the period. Management will continually analyze this metric and may include additional adjustments in the calculation in order to provide further understanding of ANI’s results. Adjusted non-GAAP diluted earnings per share should be considered in addition to, but not in lieu of, diluted earnings (loss) per share reported under GAAP. A reconciliation of adjusted non-GAAP diluted earnings per share to the most directly comparable GAAP financial measure is provided below.
ANI is not providing a reconciliation for the forward-looking full year 2026 adjusted diluted earnings per share guidance because it does not currently have sufficient information to accurately estimate all of the variables and individual adjustments for such reconciliation, including “with” and “without” tax provision information. As such, ANI’s management cannot estimate on a forward-looking basis without unreasonable effort the impact these variables and individual adjustments will have on its reported results.
Other non-GAAP metrics
ANI’s management considers non-GAAP research and development expenses and non-GAAP selling, general, and administrative expenses to be financial indicators of ANI’s operating performance, providing investors and analysts with useful measures of operating results unaffected by non-cash stock-based compensation expense, M&A transaction and integration expenses, expenses incurred and settlement payments received in connection with certain litigation matters, severance expense, and certain other items that vary in frequency and impact on ANI’s results of operations.
Management uses adjusted non-GAAP research and development expenses and non-GAAP selling, general, and administrative expenses when analyzing Company performance. Non-GAAP research and development expenses is defined as research and development expenses, excluding non-cash stock-based compensation expense, and certain other items that vary in frequency and impact on ANI’s results of operations.
Non-GAAP selling, general, and administrative expenses is defined as selling, general, and administrative expenses, excluding non-cash stock-based compensation expense, M&A transaction and integration expenses, expenses incurred and settlement payments received in connection with certain litigation matters, severance expense, and certain other items that vary in frequency and impact on ANI’s results of operations.
Each of adjusted non-GAAP research and development expenses and non-GAAP selling, general, and administrative expenses should be considered in addition to, but not in lieu of, research and development expenses, and selling, general, and administrative expenses reported under GAAP, respectively.
A reconciliation of each of non-GAAP research and development expenses and non-GAAP selling, general and administrative expenses to the most directly comparable GAAP financial measure is provided below.
ANI’s management also considers non-GAAP gross margin to be a financial indicator of ANI’s operating performance, providing investors and analysts with a useful measure of operating results unaffected by non-cash stock-based compensation expense, and certain other items that vary in frequency and impact on ANI’s results of operations. Management uses non-GAAP gross margin when analyzing Company performance.
Non-GAAP gross margin is defined as adjusted non-GAAP net revenues less non-GAAP cost of sales (excluding depreciation and amortization) divided by non-GAAP net revenues. Non-GAAP gross margin should be considered in addition to, but not in lieu of, gross margin reported under GAAP.
About ANI
ANI Pharmaceuticals, Inc. (Nasdaq: ANIP) is a diversified biopharmaceutical company committed to its mission of “Serving Patients, Improving Lives” by developing, manufacturing, and commercializing innovative and high-quality therapeutics. The Company is focused on delivering sustainable growth through its Rare Disease business, which markets novel products in the areas of ophthalmology, rheumatology, nephrology, neurology, and pulmonology; its Generics business, which leverages R&D expertise, operational excellence, and U.S.-based manufacturing; and its Brands business. For more information, visit
.
Forward-Looking Statements
To the extent any statements made in this release deal with information that is not historical, these are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements include, but are not limited to, statements regarding the Company’s strategy; its expectations regarding its future operations, financial position or revenues, including its 2026 financial guidance; its expectations regarding its share repurchase program; the results and timing of the Company’s preclinical studies, clinical trials, regulatory submissions and regulatory approvals; the commercialization and anticipated sales of the Company’s products, including current and planned product launches and any additional product launches from the Company’s generic pipeline; the Company’s estimates of the market opportunity and addressable patient populations for its products; the expansion and execution capabilities of the Company’s sales force for acute gouty arthritis for Cortrophin Gel; the Company’s anticipated growth opportunities, including for Cortrophin Gel and ILUVIEN; the Company’s positioning for continued shareholder value creation; anticipated R&D developments and clinical trial advances; and other statements that are not historical in nature, particularly those that utilize terminology such as “anticipates,” “will,” “expects,” “plans,” “potential,” “future,” “believes,” “intends,” “continue,” the negatives thereof, or other words of similar meaning, derivations of such words and the use of future dates.
Uncertainties and risks may cause the Company’s actual results to be materially different than those expressed in or implied by such forward-looking statements. Uncertainties and risks include, but are not limited to: the ability of the Company’s approved products, including Cortrophin Gel and ILUVIEN, to achieve commercialization at levels of market acceptance that will allow the Company to maintain profitability; the Company’s ability to complete or achieve any or all of the intended benefits of acquisitions and investments, in a timely manner or at all; delays and disruptions in the production of the Company’s approved products; increased costs and potential loss of revenues if the Company needs to change suppliers due to the limited number of suppliers for its raw materials, active pharmaceutical ingredients, excipients, and other materials; delays and disruptions in the production of the Company’s approved products as a result of its reliance on single source third party contract manufacturing supply for certain of its key products, including Cortrophin Gel and ILUVIEN; delays or failure to obtain or maintain approvals by the FDA of the Company’s products; changes in policy or actions that may be taken by the FDA, United States Drug Enforcement Administration and other regulatory agencies; risks that the Company may face with respect to importing raw materials and delays in delivery of raw materials and other ingredients and supplies necessary for the manufacture of the Company’s products from both domestic and overseas sources due to supply chain disruptions or for any other reason, including increased costs due to tariffs or macroeconomic disruptions; the ability of the Company’s manufacturing partners to meet its product demands and timelines; the impact of changes or fluctuations in exchange rates; the Company’s ability to develop, license or acquire, and commercialize new products; the Company’s obligations in agreements under which it licenses, develops or commercializes rights to products or technology from third parties and its ability to maintain such licenses; the level of competition the Company faces and the legal, regulatory and/or legislative strategies employed by its competitors to prevent or delay competition from generic alternatives to branded products; the Company’s ability to protect its intellectual property rights; the impact of legislative or regulatory reform on the pricing for pharmaceutical products; the impact of any litigation to which the Company is, or may become, a party; the Company’s ability, and that of its suppliers, development partners, and manufacturing partners, to comply with laws, regulations and standards that govern or affect the pharmaceutical and biotechnology industries; the Company’s ability to maintain the services of its key executives and other personnel; and general business and economic conditions, such as inflationary pressures, geopolitical conditions.
More detailed information on these and additional factors that could affect the Company’s actual results are described in the Company’s filings with the Securities and Exchange Commission (SEC), including its most recent annual report on Form 10-K and quarterly reports on Form 10-Q, and other periodic reports, as well as other filings with the SEC. All forward-looking statements in this news release speak only as of the date of this news release and are based on the Company’s current beliefs, assumptions, and expectations. The Company undertakes no obligation to update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.
Investor Relations:
Irina Koffler, Vice President, Investor Relations
T: 917-734-7387
E: Irina.koffler@anipharmaceuticals.com
Media Relations:
Argot Partners
T: 212-600-1494
E: ani@argotpartners.com
SOURCE: ANI Pharmaceuticals, Inc.
FINANCIAL TABLES FOLLOW
ANI Pharmaceuticals, Inc. and Subsidiaries
Table 1: US GAAP Statements of Operations
(unaudited, in thousands, except per share amounts)
Three Months Ended June 30,
Six Months Ended June 30,
2026
2025
2026
2025
Net Revenues
$
266,044
$
211,371
$
503,506
$
408,493
Operating Expenses
Cost of sales (excluding depreciation and amortization)
100,158
74,615
193,740
147,652
Research and development
14,747
16,535
25,347
27,099
Selling, general, and administrative
91,661
81,771
165,316
158,299
Depreciation and amortization
19,640
23,281
40,559
46,172
Contingent consideration fair value adjustment
(622
)
1,277
(804
)
(10,815
)
Total Operating Expenses, net
225,584
197,479
424,158
368,407
Operating income
40,460
13,892
79,348
40,086
Other (expense) income, net
Unrealized gain (loss) on investment in equity securities
741
332
6,494
(589
)
Interest expense, net
(3,636
)
(5,438
)
(7,405
)
(10,922
)
Other (expense) income, net
(468
)
1,739
(1,119
)
1,937
Income Before Income Tax Expense
37,097
10,525
77,318
30,512
Income tax expense
12,386
1,976
23,115
6,282
Net Income
$
24,711
$
8,549
$
54,203
$
24,230
Dividends on Series A Convertible Preferred Stock
—
(407
)
—
(813
)
Net Income Available to Common Shareholders
$
24,711
$
8,142
$
54,203
$
23,417
Basic and Diluted Income Per Share:
Basic Income Per Share
$
1.09
$
0.37
$
2.40
$
1.07
Diluted Income Per Share
$
1.05
$
0.36
$
2.32
$
1.05
Basic Weighted-Average Shares Outstanding
21,158
19,834
21,036
19,721
Diluted Weighted-Average Shares Outstanding
21,915
20,308
21,785
20,177
ANI Pharmaceuticals, Inc. and Subsidiaries
Table 2: US GAAP Balance Sheets
(unaudited, in thousands)
June 30,
2026
December 31,
2025
Assets
Current Assets
Cash and cash equivalents
$
360,212
$
285,585
Restricted cash
35
36
Accounts receivable, net
274,469
281,082
Inventories
143,149
143,067
Prepaid expenses and other current assets
31,942
34,216
Investment in equity securities
15,626
9,131
Total Current Assets
825,433
753,117
Non-current Assets
Property and equipment, net
73,223
62,476
Deferred tax assets, net
71,495
69,072
Intangible assets, net
449,857
479,526
Goodwill
62,480
62,480
Other non-current assets
11,624
13,706
Total Assets
$
1,494,112
$
1,440,377
Liabilities and Stockholders’ Equity
Current Liabilities
Accounts payable
$
73,830
$
62,583
Accrued royalties
55,830
48,497
Accrued compensation and related expenses
27,154
37,897
Accrued government rebates
41,392
43,154
Returned goods reserve
44,013
49,504
Accrued expenses and other
16,575
16,970
Income taxes payable
3,532
2,239
Current debt, net
21,329
17,268
Total Current Liabilities
283,655
278,112
Non-current Liabilities
Debt, net
280,155
291,840
Convertible notes, net
309,009
307,927
Contingent consideration
8,546
9,610
Other non-current liabilities
15,535
12,164
Total Liabilities
$
896,900
$
899,653
Stockholders’ Equity
Common Stock
3
3
Class C Special Stock
—
—
Preferred Stock
—
—
Treasury stock
(53,817
)
(33,249
)
Additional paid-in capital
620,249
596,036
Retained earnings (Accumulated deficit)
31,104
(23,099
)
Accumulated other comprehensive (loss) income, net of tax
(327
)
1,033
Total Stockholders’ Equity
597,212
540,724
Total Liabilities and Stockholders’ Equity
$
1,494,112
$
1,440,377
ANI Pharmaceuticals, Inc. and Subsidiaries
Table 3: Adjusted non-GAAP EBITDA Calculation and US GAAP to Non-GAAP Reconciliation
(unaudited, in thousands)
Reconciliation of certain adjusted non-GAAP accounts:
Net Revenues
Cost of sales (excluding depreciation and amortization)
Selling, general, and administrative
Research and development
Three Months Ended
June 30,
Three Months Ended
June 30,
Three Months Ended June 30,
Three Months Ended June 30,
Three Months Ended June 30,
2026
2025
2026
2025
2026
2025
2026
2025
2026
2025
Net Income
$
24,711
$
8,549
As reported:
$
266,044
$
211,371
$
100,158
$
74,615
$
91,661
$
81,771
$
14,747
$
16,535
Add/(Subtract):
Interest expense, net
3,636
5,438
Other expense (income), net
468
(1,739
)
Income tax expense
12,386
1,976
Depreciation and amortization
19,640
23,281
Contingent consideration fair value adjustment
(622
)
1,277
Unrealized gain on investment in equity securities
(741
)
(332
)
Stock-based compensation
11,406
9,603
Stock-based compensation
—
—
(552
)
(405
)
(10,238
)
(8,615
)
(616
)
(583
)
M&A transaction and integration expenses
40
823
M&A transaction and integration expenses
—
—
—
—
(40
)
(823
)
—
—
Litigation expenses
673
5,201
Litigation expenses
—
—
—
—
(673
)
(5,201
)
—
—
Adjusted non-GAAP EBITDA
$
71,597
$
54,077
As adjusted:
$
266,044
$
211,371
$
99,606
$
74,210
$
80,710
$
67,132
$
14,131
$
15,952
Reconciliation of certain adjusted non-GAAP accounts:
Net Revenues
Cost of sales (excluding depreciation and amortization)
Selling, general, and administrative
Research and
development
Six Months Ended
June 30,
Six Months Ended
June 30,
Six Months Ended
June 30,
Six Months Ended
June 30,
Six Months Ended
June 30,
2026
2025
2026
2025
2026
2025
2026
2025
2026
2025
Net Income
$
54,203
$
24,230
As reported:
$
503,506
$
408,493
$
193,740
$
147,652
$
165,316
$
158,299
$
25,347
$
27,099
Add/(Subtract):
Interest expense, net
7,405
10,922
Other expense (income), net
1,119
(1,937
)
Income tax expense
23,115
6,282
Depreciation and amortization
40,559
46,172
Contingent consideration fair value adjustment
(804
)
(10,815
)
Unrealized (gain) loss on investment in equity securities
(6,494
)
589
Stock-based compensation
21,597
18,470
Stock-based compensation
—
—
(1,047
)
(780
)
(19,310
)
(16,581
)
(1,240
)
(1,109
)
M&A transaction and integration expenses
301
2,617
M&A transaction and integration expenses
—
—
—
—
(301
)
(2,617
)
—
—
Litigation expenses and settlement proceeds
(6,407
)
8,192
Litigation expenses and settlement proceeds
—
—
—
—
6,407
(8,192
)
—
—
Severance
—
105
Severance
—
—
—
—
—
(105
)
—
—
Adjusted non-GAAP EBITDA
$
134,594
$
104,827
As adjusted:
$
503,506
$
408,493
$
192,693
$
146,872
$
152,112
$
130,804
$
24,107
$
25,990
ANI Pharmaceuticals, Inc. and Subsidiaries
Table 4: US GAAP Gross Margin to Non-GAAP Gross Margin Reconciliation
(unaudited, in thousands)
Three Months Ended June 30,
Six Months Ended June 30,
2026
2025
2026
2025
GAAP net revenues
$
266,044
$
211,371
$
503,506
$
408,493
GAAP cost of sales (excluding depreciation and amortization)
100,158
74,615
193,740
147,652
GAAP gross profit
$
165,886
$
136,756
$
309,766
$
260,841
Stock-based compensation
552
405
1,047
780
Non-GAAP gross profit
$
166,438
$
137,161
$
310,813
$
261,621
GAAP gross margin
62.4
%
64.7
%
61.5
%
63.9
%
Non-GAAP gross margin
62.6
%
64.9
%
61.7
%
64.0
%
ANI Pharmaceuticals, Inc. and Subsidiaries
Table 5: Adjusted non-GAAP Net Income and Adjusted non-GAAP Diluted Earnings per Share Reconciliation
(unaudited, in thousands, except per share amounts)
Three Months Ended June 30,
Six Months Ended June 30,
2026
2025
2026
2025
Net Income Available to Common Shareholders
$
24,711
$
8,142
$
54,203
$
23,417
Add/(Subtract):
Non-cash interest expense
137
252
354
511
Depreciation and amortization
19,640
23,281
40,559
46,172
Contingent consideration fair value adjustment
(622
)
1,277
(804
)
(10,815
)
Unrealized (gain) loss on investment in equity securities
(741
)
(332
)
(6,494
)
589
Stock-based compensation
11,406
9,603
21,597
18,470
M&A transaction and integration expenses
40
823
301
2,617
Litigation expenses and settlement proceeds
673
5,201
(6,407
)
8,192
Severance
—
—
—
105
Other expense (income)
442
(1,773
)
1,104
(2,009
)
Less:
Estimated tax impact of adjustments
(8,054
)
(9,966
)
(13,055
)
(16,596
)
Adjusted non-GAAP Net Income Available to Common Shareholders
(1)
$
47,632
$
36,508
$
91,358
$
70,653
Diluted Weighted-Average
Shares Outstanding
21,915
20,308
21,785
20,177
Adjusted Diluted Weighted-Average
(2)
Shares Outstanding
21,575
20,308
21,440
20,177
Adjusted non-GAAP
Diluted Earnings per Share
$
2.21
$
1.80
$
4.26
$
3.50
(1)
Adjusted non-GAAP Net Income Available to Common Shareholders excludes undistributed earnings to participating securities.
(2)
Non-GAAP Adjusted Diluted Weighted-Average Shares Outstanding exclude certain dilutive shares related to the senior convertible notes as they are intended to be covered by our capped call transactions. Our outstanding capped call transactions are intended to fully offset the dilutive effect of the senior convertible notes recognized in the calculation of GAAP diluted EPS, and therefore 340,000 shares and 345,000 shares, for the three and six months ended June 30, 2026, respectively, have been excluded from the calculation of Non-GAAP Adjusted Diluted Weighted-Average Shares Outstanding.
