Cumberland Q3 net income: $77.8M with disposal gain
Cumberland says its planned DMD application will include safety data from more than 1,400 subjects across approximately 30 clinical studies.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Form Type
8-K
Rhea-AI Filing Summary
Cumberland Pharmaceuticals reported third-quarter 2026 net income of $77.8 million, including an $81.1 million gain on disposal tied to its July 1, 2026 strategic transaction with Apotex Health. The transaction closed with $100 million in proceeds; Cumberland's commercial brands and organization were integrated into Apotex's U.S. branded business. Total revenue was $2.16 million versus $171,821 in Q3 2025; continuing operations recorded a $1.12 million net loss.
At September 30, 2026, cash and cash equivalents were $80.6 million, total assets were $113.8 million, liabilities were $41.6 million and shareholders' equity was $72.5 million. In the first nine months, operating activities used $942,253 in cash, versus $4.93 million provided in 2025.
Cumberland plans to submit an NDA for ifetroban for DMD cardiomyopathy; the FDA granted rolling review, allowing completed sections to be submitted before the full application. In the Phase 2 FIGHT DMD trial, the high-dose group showed a statistically significant 5.4-percentage-point improvement in left ventricular ejection fraction versus a control group combining placebo-treated patients with propensity score-matched natural-history patients (p=0.002). In the Phase 2a systemic sclerosis trial, no serious adverse event during 12-month treatment was assessed as related to ifetroban; planned biomarker and cardiac-imaging analyses will inform the company's decision on further development.
3 points · 1 major0 major · 1 point
How this balance works
Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.
It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.
Rhea-AI Sentiment measures something else, the tone of the wording.
Positive
- Major pointStrategic transaction closed with $100 million in proceeds. 1.3× market cap
- Moderate pointRevenue totaled $2.16 million versus $171,821 in Q3 2025.
- Minor pointNet income was $77.8 million, including an $81.1 million disposal gain.
Negative
- Moderate pointOperating cash flow: $942,253 used in nine months, versus $4.93 million provided.
Filing Explained
Through September 30, 2026, continuing operations used $1,133,984 in operating cash, and $22,479,497 in dividends had been paid.
The 8-K’s nine-month cash-flow statement separates continuing from discontinued operations: continuing operations used
The statement also records
8-K Event Classification
2 items: 2.02, 9.01
2 items
Item 2.02
Results of Operations and Financial Condition
Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01
Financial Statements and Exhibits
Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Key Figures
Total revenue: $2.16 million
Net income: $77.8 million
Gain on disposal: $81.1 million
+4 more
7 metrics
Total revenue
$2.16 million
Three months ended September 30, 2026; $171,821 in the 2025 period
Net income
$77.8 million
Three months ended September 30, 2026; includes an $81.1 million gain on disposal
Gain on disposal
$81.1 million
Three months ended September 30, 2026
Transaction proceeds
$100 million
At closing on July 1, 2026
Cash and cash equivalents
$80.6 million
As of September 30, 2026
Operating cash flow
$942,253 used
Nine months ended September 30, 2026; $4.93 million provided in the 2025 period
Left ventricular ejection fraction improvement
5.4 percentage points
High-dose group versus the control group; p=0.002
Key Terms
New Drug Application, rolling review, left ventricular ejection fraction, propensity score-matched natural history patients, +1 more
5 terms
New Drug Application regulatory
"submit a New Drug Application"
A new drug application is a formal request submitted to government regulators seeking approval to market a new medicine. It is like a detailed proposal that shows the drug has been tested for safety and effectiveness. For investors, receiving approval signals that the drug may soon become available for sale, potentially leading to revenue growth and impacting the company's value.
rolling review regulatory
"rolling review, which allows completed sections"
A rolling review is a regulatory process where health authorities examine data on a drug or vaccine as it becomes available instead of waiting for a complete file at the end. For investors, this can speed up the timeline to approval and reduce uncertainty because regulators assess progress in real time—think of reading and approving chapters of a book as they’re finished rather than waiting for the whole manuscript, which can bring forward potential market access and revenue.
left ventricular ejection fraction medical
"improvement in left ventricular ejection fraction"
Left ventricular ejection fraction (LVEF) is the percentage of blood the heart’s main pumping chamber pushes out with each beat, measured by comparing the volume before and after contraction. Think of it as how much water a pump empties from a tank each cycle — higher percentages mean stronger pumping. Investors care because LVEF is a common clinical measure that affects patient outcomes, market size for treatments, trial success, reimbursement and regulatory decisions in healthcare-related investments.
propensity score-matched natural history patients technical
"propensity score-matched natural history patients"
discontinued operations financial
"revenues and expenses associated with the Strategic Transaction continued to be classified as discontinued operations"
Discontinued operations are parts of a company that it has decided to sell or shut down, and no longer plans to run in the future. This matters to investors because it helps them understand which parts of the business are ongoing and which are being phased out, providing a clearer picture of the company’s current performance and future prospects. Think of it like a store closing a department—it no longer contributes to sales or profits.
Earnings Snapshot
Total revenue: $2.16 million
Three months ended September 30, 2026
Total revenue
$2.16 million
From $171,821 in the three months ended September 30, 2025
Net income
$77.8 million
From a net loss of $1.95 million in the three months ended September 30, 2025
Net income from continuing operations
A net loss of $1.12 million
Versus a net loss of $2.73 million in the three months ended September 30, 2025
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.
What were CPIX's third-quarter 2026 results?
CPIX reported $77.8 million in third-quarter net income, including an $81.1 million gain on disposal, and $2.16 million in total revenue; continuing operations recorded a $1.12 million net loss.
What did CPIX's Phase 2 DMD trial show?
The high-dose group showed a statistically significant 5.4-percentage-point improvement in left ventricular ejection fraction versus a control group combining placebo-treated patients with propensity score-matched natural-history patients (p=0.002). Cumberland plans an NDA submission for ifetroban for DMD cardiomyopathy, and the FDA granted rolling review.
AI-generated analysis. How Rhea-AI works. Not financial advice.
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 OR 15(d) of The Securities Exchange Act of 1934
Date of Report (date of earliest event reported)
(Exact name of registrant as specified in its charter)
(State or other jurisdiction of incorporation or organization) | (Commission File Number) | (I.R.S. Employer Identification No.) | |||||||||
(Address of Principal Executive Offices)
(615 ) 255-0068
Registrant's telephone number, including area code
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered | ||||||
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
Item 2.02 Results of Operations and Financial Condition.
On November 10, 2026 , Cumberland Pharmaceuticals Inc. (the "Company") issued a press release which provided a company update and the financial results for the three and nine months ended September 30, 2026. A copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated by reference into this Item 2.02.
This information is furnished pursuant to Item 2.02 of Form 8-K and shall not be deemed filed for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), or otherwise subject to the liabilities of that section, unless specifically incorporated by reference in a document filed under the Securities Act of 1933, as amended, or the Exchange Act. By filing this report on Form 8-K and furnishing this information, the Company makes no admission as to the materiality of any information in this report that is required to be disclosed solely by Item 2.02.
Item 9.01 Financial Statements and Exhibits
(d) Exhibits
| Exhibit No. | Description | |||||||
99.1 | Press release dated November 10, 2026 | |||||||
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| Cumberland Pharmaceuticals Inc. | ||||||||||||||||||||
Dated: | By: | /s/ John Hamm | ||||||||||||||||||
| John Hamm | ||||||||||||||||||||
| Chief Financial Officer | ||||||||||||||||||||
CUMBERLAND PHARMACEUTICALS REPORTS
Q3 2026 FINANCIAL RESULTS & COMPANY UPDATE
$100 million Strategic Transaction Closed
Plans to Submit New Drug Application for Ifetroban in DMD
Top-Line Results Announced for Systemic Sclerosis Trial
NASHVILLE, Tenn. (Nov. 10, 2026) – Cumberland Pharmaceuticals Inc. (Nasdaq: CPIX), an innovation-focused biopharmaceutical company developing new products for rare diseases, announced today its third quarter 2026 financial results and provided a company update. Cumberland has announced its decision to submit a New Drug Application (“NDA”) to the U.S. Food and Drug Administration (“FDA”) for ifetroban as a potential treatment for the cardiomyopathy associated with Duchenne muscular dystrophy (“DMD”).
The third quarter of 2026 marked Cumberland’s first period of operations following the July 1, 2026, closing of its Strategic Transaction with Apotex Health, the largest pharmaceutical company based in Canada. Cumberland’s commercial brands and organization were integrated into Apotex’s U.S. branded business. The $100 million in proceeds at closing strengthened the company’s balance sheet, simplified its business model and allowed Cumberland to concentrate its resources on its clinical pipeline.
“Our first full quarter as a development-focused company has reinforced the value of concentrating our efforts on our clinical pipeline,” said A.J. Kazimi, CEO of Cumberland Pharmaceuticals. “Our team and resources are now dedicated to developing new medicines for unmet medical needs. We have the financial strength and the expertise to pursue our new mission, as we work to create lasting value for patients and shareholders.”
RECENT COMPANY DEVELOPMENTS INCLUDE:
Plans to File New Drug Application for Ifetroban in DMD
Cumberland announced its decision to submit an NDA to the FDA for ifetroban as a potential treatment for the cardiomyopathy associated with DMD, a rare, fatal genetic neuromuscular disease that results in deterioration of the skeletal, heart and lung muscles. The decision follows a pre-NDA meeting with the FDA this fall. The FDA granted Cumberland’s request for a rolling review, which allows completed sections of the application to be submitted for review before the entire application is filed.
The submission will be supported by data from the Phase 2 FIGHT DMD® trial, which demonstrated a statistically significant 5.4 percentage point improvement in left ventricular ejection fraction (p=0.002) in the high-dose group compared with a control group of placebo-treated patients combined with propensity score-matched natural history patients. Findings also included a reduction in markers of cardiac damage. The NDA submission will also include long-term data from the ongoing open-label extension, preclinical data published in the Journal of the American Heart Association, manufacturing information and a safety database of more than 1,400 subjects across approximately 30 clinical studies.
Through up to 36 months of treatment across the Phase 2 trial and its open-label extension, ifetroban has maintained a favorable safety profile in DMD patients, with no treatment-related serious adverse events or new safety concerns.
There is currently no approved therapy specifically targeting DMD heart disease, the leading cause of death in these patients. Ifetroban has received Orphan Drug, Rare Pediatric Disease and Fast Track designations, and the FDA has conditionally accepted DYSCORBAN® as the proprietary name for the product. Cumberland has also secured a growing portfolio of patents protecting ifetroban for this DMD heart disease indication.
Top-Line Results from Phase 2 Systemic Sclerosis Trial
Cumberland announced top-line results from its Phase 2a ASSIST-SSc trial evaluating ifetroban in patients with Systemic Sclerosis (SSc), a debilitating autoimmune disease characterized by diffuse fibrosis of the skin and internal organs, with no approved therapy for the underlying condition. Ifetroban was generally well tolerated, with a safety profile consistent with prior experience, and no serious adverse event during the 12-month treatment period was assessed as related to study drug.
As next steps, Cumberland plans to submit the clinical study report to the FDA and complete correlative biomarker studies using specimens collected during the trial, along with cardiac imaging evaluations from patients continuing in the open-label extension. These findings will inform the company’s decision on further development of ifetroban in SSc.
New Mission Reflects Focus on Innovation
Following the Strategic Transaction, Cumberland completed a strategic planning process to take a fresh look at who the company is and where it is headed.
The result is a refined mission statement that reflects the company’s emphasis on innovation:
Advancing new therapies that address significant unmet medical needs.
The mission guides Cumberland’s next chapter as an innovation-focused biopharmaceutical company developing new products for rare diseases. It centers the company’s resources and expertise on advancing its clinical-stage pipeline, led by ifetroban, while continuing to build on its experience developing and delivering differentiated medicines for patients.
FINANCIAL RESULTS:
Net Income: During the third quarter of 2026, the revenues and expenses associated with the Strategic Transaction continued to be classified as discontinued operations. Net income for the quarter was $77.8 million, which included the gain on divestiture of the assets associated with the Strategic Transaction, along with the ongoing investment in research and development, supported by the remaining general and administrative expenses.
Balance Sheet: At September 30, 2026, Cumberland had approximately $114 million in total assets, including $80.6 million in cash and cash equivalents. Liabilities totaled $42 million and total shareholders’ equity was $73 million as of September 30, 2026.
EARNINGS REPORT CALL:
A conference call will be held today, November 10, 2026, at 4:30 p.m. Eastern Time to provide a company update and discuss the financial results.
The link to register is https://register-conf.media-server.com/register/BI0050c03d0ef44b49b8905264f4232aef.
Registered participants can dial in from their phone using a dial-in and PIN number that will be provided to them. Alternatively, they can choose a “Call Me” option to have the system automatically call them at the start of the conference.
A replay of the call will be available for one year and can be accessed via the Investor Relations page of Cumberland’s website or by visiting https://edge.media-server.com/mmc/p/nbwu96yx.
About Cumberland Pharmaceuticals
Cumberland Pharmaceuticals Inc. is an innovation-focused biopharmaceutical company developing new therapies to address significant unmet medical needs and improve the patient outcomes. The Company is advancing a clinical pipeline of late-stage product candidates across multiple therapeutic areas with significant unmet medical needs.
Cumberland's Phase 2 clinical programs are also evaluating ifetroban in patients with Idiopathic Pulmonary Fibrosis and Cancer Metastasis. Top-line results from a Phase 2 study in patients with Systemic Sclerosis were recently announced.
For more information, please visit www.cumberlandpharma.com.
FORWARD LOOKING STATEMENTS:
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by words such as “may,” “will,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “potential,” “continue,” “could,” “should,” “would” and similar expressions, although not all forward-looking statements contain these words. These statements include, among others, statements regarding the timing, content and completion of the NDA submission, including the rolling review; Cumberland's plan to seek approval based on the FIGHT DMD™ trial and natural history data without conducting additional trials; the results of the ongoing open-label extension analyses; regulatory review, approval and labeling; the potential benefits of Orphan Drug, Rare Pediatric Disease, including eligibility for a priority review voucher, and Fast Track designations, which may not be realized; the proprietary name; patent protection and exclusivity; manufacturing; commercialization and market acceptance; the need for additional capital; competition; reliance on third parties; and other ifetroban programs. These statements are based on current assumptions and plans of Cumberland's management and are subject to risks, uncertainties, assumptions and other factors that could cause actual results to differ materially from those expressed or implied by the forward-looking statements. Important factors that could cause such differences include, among others, the risk that FDA will refuse to file the NDA or will not approve ifetroban; the risk that FDA will not agree with Cumberland's interpretation of the minutes or outcomes of its meetings with FDA; the risk that FDA will require additional trials and data, which could significantly delay or prevent approval and require substantial additional capital; the risk that additional data may not be favorable; Cumberland's ability to meet FDA's other approval requirements, including chemistry, manufacturing and controls requirements; the risk that rolling review will not shorten the review timeline; restrictions that may be placed on the label, if approved; changes in FDA requirements, policies or regulatory pathways; and the risks described under the heading "Risk Factors" in Cumberland's most recent Form 10-K and subsequent Form 10-Q filings, as well as other reports filed with the Securities and Exchange Commission. You should not place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Cumberland undertakes no obligation to update any forward-looking statement except as required by law.
SOURCE: Cumberland Pharmaceuticals Inc.
Investor Contact: | Media Contact: | ||||
Shayla Simpson | Emily Kent | ||||
Cumberland Pharmaceuticals Inc. | Dalton Agency | ||||
(615) 255-0068 | (540) 621-5448 | ||||
- MORE -
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES
Condensed Consolidated Balance Sheets
(Unaudited)
| September 30, 2026 | December 31, 2025 | ||||||||||
| ASSETS | |||||||||||
| Current assets: | |||||||||||
| Cash and cash equivalents | $ | 80,581,021 | $ | 11,444,693 | |||||||
| Accounts receivable, net | 2,132,107 | 16,944,780 | |||||||||
| Accounts receivable - TSA, net | 10,373,965 | — | |||||||||
| Receivable from Apotex | 10,617,805 | — | |||||||||
| Inventories, net | 29,935 | 29,935 | |||||||||
| Prepaid and other current assets | 634,174 | 654,166 | |||||||||
| Current assets of discontinued operations | 191,731 | 7,986,693 | |||||||||
| Total current assets | 104,560,738 | 37,060,267 | |||||||||
| Non-current inventories | 42,230 | 40,879 | |||||||||
| Property and equipment, net | 232,154 | 264,724 | |||||||||
| Intangible assets, net | 35,471 | 53,621 | |||||||||
| Operating lease right-of-use assets | 7,188,055 | 5,781,728 | |||||||||
| Other assets | 1,720,645 | 2,973,378 | |||||||||
| Assets of discontinued operations | — | 30,649,395 | |||||||||
| Total assets | $ | 113,779,293 | $ | 76,823,992 | |||||||
| LIABILITIES AND EQUITY | |||||||||||
| Current liabilities: | |||||||||||
| Accounts payable | $ | 16,502,496 | $ | 18,567,546 | |||||||
| Payable to Apotex | 6,889,538 | — | |||||||||
| Operating lease current liabilities | 521,323 | 467,774 | |||||||||
| Pre-close accrued liabilities | — | 7,774,143 | |||||||||
| Other current liabilities | 6,462,094 | 2,855,952 | |||||||||
| Other current liabilities - TSA | 3,954,134 | — | |||||||||
| Current liabilities of discontinued operations | — | 7,079,504 | |||||||||
| Total current liabilities | 34,329,585 | 36,744,919 | |||||||||
| Revolving line of credit - long term | — | 5,240,733 | |||||||||
| Operating lease non-current liabilities | 4,074,445 | 4,471,965 | |||||||||
| Other long-term liabilities | 3,200,097 | 3,626,875 | |||||||||
| Liabilities of discontinued operations | — | 2,195,278 | |||||||||
| Total liabilities | 41,604,127 | 52,279,770 | |||||||||
| Equity: | |||||||||||
| Shareholders’ equity: | |||||||||||
| Common stock— no par value; 100,000,000 shares authorized; 14,992,812 and 14,956,627 shares issued and outstanding as of September 30, 2026, and December 31, 2025, respectively | 51,578,550 | 51,684,381 | |||||||||
| Accumulated earnings (deficit) | 20,927,415 | (26,804,059) | |||||||||
| Total shareholders’ equity | 72,505,965 | 24,880,322 | |||||||||
| Noncontrolling interests | (330,799) | (336,100) | |||||||||
| Total equity | 72,175,166 | 24,544,222 | |||||||||
| Total liabilities and equity | $ | 113,779,293 | $ | 76,823,992 | |||||||
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Operations
(Unaudited)
| Three months ended September 30, | Nine months ended September 30, | ||||||||||||||||||||||
| 2026 | 2025 | 2026 | 2025 | ||||||||||||||||||||
| Transition services revenue | $ | 1,950,000 | $ | 171,821 | $ | 1,950,000 | $ | 719,247 | |||||||||||||||
| Net revenue | 206,356 | — | 536,665 | — | |||||||||||||||||||
| Total revenue | 2,156,356 | 171,821 | 2,486,665 | 719,247 | |||||||||||||||||||
| Costs and expenses: | |||||||||||||||||||||||
| Cost of transition services | 1,062,266 | — | 1,062,266 | — | |||||||||||||||||||
| Research and development | 841,162 | 646,473 | 2,379,170 | 2,178,866 | |||||||||||||||||||
| General and administrative | 2,182,285 | 2,376,284 | 7,128,677 | 7,244,245 | |||||||||||||||||||
| Amortization | 7,125 | 5,586 | 21,276 | 17,430 | |||||||||||||||||||
| Total costs and expenses | 4,092,838 | 3,028,343 | 10,591,389 | 9,440,541 | |||||||||||||||||||
| Operating loss | (1,936,482) | (2,856,522) | (8,104,724) | (8,721,294) | |||||||||||||||||||
| Interest income | 822,886 | 131,583 | 961,802 | 384,781 | |||||||||||||||||||
| Interest expense | (4,604) | (29) | (5,394) | (4,892) | |||||||||||||||||||
| Loss before income taxes | (1,118,200) | (2,724,968) | (7,148,316) | (8,341,405) | |||||||||||||||||||
| Income tax expense | (3,871) | (5,670) | (11,611) | (17,011) | |||||||||||||||||||
| Net loss from continuing operations | (1,122,071) | (2,730,638) | (7,159,927) | (8,358,416) | |||||||||||||||||||
| Discontinued operations: | |||||||||||||||||||||||
| Income (loss) from discontinued operations | (1,725,098) | 781,592 | (3,248,722) | 6,922,347 | |||||||||||||||||||
| Gain on disposal of discontinued operations | 81,092,578 | — | 81,092,578 | — | |||||||||||||||||||
| Income tax expense on disposal of discontinued operations | (467,657) | — | (467,657) | — | |||||||||||||||||||
| Net income of discontinued operations | 78,899,823 | 781,592 | 77,376,199 | 6,922,347 | |||||||||||||||||||
| Net income (loss) | 77,777,752 | (1,949,046) | 70,216,272 | (1,436,069) | |||||||||||||||||||
| Net income (loss) at subsidiary attributable to noncontrolling interests | (766) | 8,282 | (5,301) | 11,633 | |||||||||||||||||||
| Net income (loss) attributable to common shareholders | $ | 77,776,986 | $ | (1,940,764) | $ | 70,210,971 | $ | (1,424,436) | |||||||||||||||
| Income (loss) per share attributable to common shareholders | |||||||||||||||||||||||
| - Continuing operations - basic | $ | (0.07) | $ | (0.18) | $ | (0.48) | $ | (0.56) | |||||||||||||||
| - Discontinued operations - basic | 5.26 | 0.05 | 5.17 | 0.46 | |||||||||||||||||||
| $ | 5.19 | $ | (0.13) | $ | 4.69 | $ | (0.10) | ||||||||||||||||
| - Continuing operations - diluted | $ | (0.07) | $ | (0.18) | $ | (0.46) | $ | (0.56) | |||||||||||||||
| - Discontinued operations - diluted | 5.14 | 0.05 | 5.06 | 0.46 | |||||||||||||||||||
| $ | 5.07 | $ | (0.13) | $ | 4.60 | $ | (0.10) | ||||||||||||||||
| Weighted-average shares outstanding | |||||||||||||||||||||||
| - basic | 14,989,763 | 14,958,534 | 14,977,899 | 14,953,944 | |||||||||||||||||||
| - diluted | 15,342,174 | 14,958,534 | 15,278,850 | 14,953,944 | |||||||||||||||||||
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Cash Flows
(Unaudited)
| Nine months ended September 30, | |||||||||||
| 2026 | 2025 | ||||||||||
| Cash flows from operating activities: | |||||||||||
| Net income (loss) | $ | 70,216,272 | $ | (1,436,069) | |||||||
| Gain on disposal of discontinued operations | (80,624,921) | — | |||||||||
| Adjustments to reconcile net income (loss) to net cash provided by operating activities: | |||||||||||
| Depreciation and amortization expense | 101,923 | 99,324 | |||||||||
| Amortization of operating lease right-of-use asset | 721,984 | 721,984 | |||||||||
| Share-based compensation | 192,791 | 236,160 | |||||||||
| Increase in cash surrender value of life insurance policies over premiums paid | (79,198) | (131,967) | |||||||||
| Net changes in assets and liabilities affecting operating activities: | |||||||||||
| Accounts receivable | 1,503,059 | 1,270,864 | |||||||||
| Inventories, net | — | 101,652 | |||||||||
| Other current assets and other assets | 1,356,318 | (192,899) | |||||||||
| Operating lease liabilities | (679,803) | (662,118) | |||||||||
| Accounts payable and other current liabilities | 6,584,369 | (2,587,613) | |||||||||
| Other long-term liabilities | (426,778) | 59,764 | |||||||||
| Net cash used in operating activities from continuing operations | (1,133,984) | (2,520,918) | |||||||||
| Discontinued operations | 191,731 | 7,450,415 | |||||||||
| Net cash provided by (used in) operating activities | (942,253) | 4,929,497 | |||||||||
| Cash flows from investing activities: | |||||||||||
| Additions to property and equipment | (48,095) | (97,905) | |||||||||
| Investment in cash surrender value of life insurance policies | (42,018) | — | |||||||||
| Net (increase) decrease of investment in manufacturing | (1,792,479) | (580,866) | |||||||||
| Additions to intangible assets | (5,757) | (807) | |||||||||
| Net cash used in investing activities from continuing operations | (1,888,349) | (679,577) | |||||||||
| Discontinued operations | 99,984,255 | (953,582) | |||||||||
| Net cash provided by (used in) investing activities | 98,095,906 | (1,633,159) | |||||||||
| Cash flows from financing activities: | |||||||||||
| Proceeds from ATM offering, net | — | 5,266,334 | |||||||||
| Payments on line of credit | (5,240,733) | (10,035,437) | |||||||||
| Exercise of options and purchases of shares from employees | 21,725 | — | |||||||||
| Cash dividend paid | (22,479,497) | — | |||||||||
| Payments made in connection with repurchase of common shares | (318,820) | (263,478) | |||||||||
| Net cash used in financing activities from continuing operations | (28,017,325) | (5,032,581) | |||||||||
| Discontinued operations | — | (1,031,197) | |||||||||
| Net cash used in financing activities | (28,017,325) | (6,063,778) | |||||||||
| Net increase (decrease) in cash and cash equivalents | 69,136,328 | (2,767,439) | |||||||||
| Cash and cash equivalents at beginning of period | 11,444,693 | 17,964,184 | |||||||||
| Cash and cash equivalents at end of period | $ | 80,581,021 | $ | 15,196,745 | |||||||