Company Description
Organon & Co. (NYSE: OGN) is a global healthcare company that focuses on pharmaceutical preparation manufacturing within women’s health and general medicines. The company describes its mission as delivering impactful medicines and solutions for a healthier every day. Organon reports a portfolio of over 70 products across Women’s Health and General Medicines, which includes biosimilars, and emphasizes addressing health needs that uniquely, disproportionately or differently affect women, while expanding access to essential treatments in more than 140 markets worldwide. Organon is headquartered in Jersey City, New Jersey.
According to the company’s own descriptions in multiple press releases, Organon’s business is organized around women’s health therapies, a broad general medicines portfolio, and a growing range of biosimilars. The Polygon profile further notes three main product portfolio groupings: women’s health, biosimilars and established medicines, and states that the majority of revenue is generated from the Established Brands product portfolio. Polygon data also indicates that Organon derives a majority of its revenue from Europe and Canada, followed by the United States and then Asia Pacific and Japan.
Within women’s health, Organon highlights products and solutions aimed at conditions that affect women in distinctive ways. Company disclosures reference contraceptive products such as Nexplanon, NuvaRing, Marvelon and Mercilon, as well as the JADA System, a medical device for control and treatment of abnormal postpartum uterine bleeding or hemorrhage when conservative management is warranted. Organon has also announced an agreement to divest the JADA System to Laborie Medical Technologies Corp., explaining that this move is intended to improve balance sheet capacity for future investment in women’s health biopharma and other strategic priorities.
In general medicines, Organon manages a diverse set of established brands and newer assets. The company’s quarterly earnings release describes an Established Brands portfolio that includes respiratory products such as Singulair and Dulera, as well as other therapies that have experienced loss of exclusivity in key markets. Organon also reports revenue contribution from products such as Emgality and Vtama, which entered the portfolio through licensing and acquisition transactions. The company’s disclosures show that established brands remain a major revenue driver, even as Organon invests in newer growth areas.
Biosimilars are a central growth pillar for Organon. The company’s communications describe a biosimilars portfolio that spans multiple therapeutic areas, including oncology, immunology and bone health. Organon reports strong performance from biosimilars such as Hadlima (adalimumab-bwwd) and Ontruzant (trastuzumab-dttb), and notes that new assets like BILDYOS (denosumab-nxxp), BILPREVDA (denosumab-nxxp) and Tofidence (tocilizumab-bavi) have begun contributing to revenue. Organon has entered into license and supply agreements with Shanghai Henlius Biotech, Inc. that grant Organon exclusive commercialization rights (outside China) to several biosimilars, including BILDYOS, BILPREVDA and POHERDY.
Regulatory milestones underline Organon’s role in biosimilars. Press releases describe US Food and Drug Administration approvals for BILDYOS and BILPREVDA as biosimilars to PROLIA and XGEVA, respectively, for all indications of the reference products. Organon and Henlius have also announced European Commission marketing authorizations for BILDYOS and BILPREVDA for all EU indications of the reference medicines. In another collaboration milestone, Organon and Henlius reported US FDA approval of POHERDY (pertuzumab-dpzb), an interchangeable biosimilar to PERJETA (pertuzumab) for all indications of the reference product, focused on HER2-positive breast cancer.
Beyond biosimilars, Organon’s general medicines portfolio includes dermatology and neurology assets. The company highlights VTAMA (tapinarof) cream, 1%, an aryl hydrocarbon receptor agonist indicated for the topical treatment of plaque psoriasis in adults and atopic dermatitis in adults and pediatric patients 2 years of age and older. Organon has presented Phase 3 data from the ADORING program showing early and consistent responses in children aged 2–17 with atopic dermatitis, including those with associated comorbidities. The company also reports European licensing and distribution rights to Emgality and Rayvow from Eli Lilly in certain markets, and notes that these products contribute to Established Brands revenue.
Organon’s financial disclosures for the third quarter of 2025 illustrate how these portfolios translate into revenue. The company reports revenue across three primary groupings: Women’s Health, Biosimilars and Established Brands, with an additional category for other items such as manufacturing sales to third parties. Women’s Health revenue reflects performance of contraceptive and related products, Biosimilars revenue is driven by assets like Hadlima and Ontruzant and newer biosimilars such as BILDYOS, BILPREVDA and Tofidence, and Established Brands revenue includes a range of legacy therapies and newer licensed products.
Geographically, Polygon data indicates that Organon generates most of its revenue from Europe and Canada, followed by the United States and then Asia Pacific and Japan. The company’s own press releases emphasize its reach into more than 140 markets, and specific agreements—such as the commercialization of Nilemdo (bempedoic acid) in France, Denmark, Iceland, Sweden, Finland and Norway—illustrate how Organon uses regional partnerships to expand access to treatments. In the Nilemdo agreement, Organon will distribute and promote the product in those European markets while Daiichi Sankyo Europe remains the marketing authorization holder.
Organon’s public communications also describe its capital allocation and balance sheet priorities. In its third quarter 2025 results, the company discusses free cash flow generation, cost discipline and proactive debt reduction as tools to create additional balance sheet capacity. The announced divestiture of the JADA System to Laborie includes a statement that net proceeds will be applied to debt reduction, consistent with an ongoing deleveraging effort. Organon’s Board of Directors has also declared quarterly dividends, as reflected in the earnings release.
Corporate governance and internal controls are another area of focus in recent filings. An 8-K filed on October 27, 2025, and related press releases describe an Audit Committee investigation into wholesaler sales practices for Nexplanon in the United States. The investigation found that certain wholesalers were asked to purchase greater quantities of Nexplanon than they otherwise would have during specified periods, and that these practices enabled Organon to meet guidance and certain external revenue expectations. The Board determined that these practices were improper and that certain prior statements were inaccurate or incomplete, although the company concluded that no restatement or revision of previously issued financial statements was required. Organon has disclosed that it is taking remedial actions to improve financial controls and address material weaknesses in internal control over financial reporting.
Leadership changes have accompanied these governance developments. The same 8-K and subsequent filings report that the Chief Executive Officer resigned in connection with the investigation, and that Joseph Morrissey, previously Executive Vice President and Head of Manufacturing & Supply, was appointed Interim Chief Executive Officer. The Board Chair, Carrie S. Cox, has taken on additional responsibilities as Executive Chair on an interim basis, and the Board has formed a search committee and engaged a search firm to identify a permanent CEO. An 8-K/A filed on October 30, 2025, discloses compensation arrangements for the Executive Chair role.
Organon’s SEC filings also show ongoing engagement with investors and regulators. The company regularly files Forms 8-K to furnish earnings releases and investor presentations, and to report material events such as board changes and investigation findings. These filings reference non-GAAP financial measures such as Adjusted EBITDA, Adjusted gross margin and Adjusted net income, and include reconciliations and cautionary notes about the limitations of non-GAAP metrics.
Overall, Organon & Co. presents itself as a global healthcare manufacturer with three main commercial pillars—women’s health, biosimilars and established medicines—supported by a broad geographic footprint and a portfolio of more than 70 products. Its disclosures emphasize a mission centered on women’s health needs and expanded access to essential treatments, while its SEC filings and press releases provide detail on product approvals, collaborations, financial performance, governance matters and capital allocation priorities.