Zydus and MSN launch the first US generic version of Adempas for pulmonary hypertension.

Zydus Lifesciences and MSN Laboratories have launched the first U.S. generic version of Adempas (riociguat), FDA-approved in five strengths for adults with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension. MSN developed and manufactures the tablets, while Zydus brings its U.S. commercial reach; the companies say the launch can expand access with a generic alternative to the previously branded-only treatment. The launch may affect market pricing and access, though the sources provide no specific generic price or sales outlook.
Bayer reported global Adempas sales of about €745 million in 2025, equivalent to roughly US$850 million, offering a measure of the branded drug’s existing market.
The articles describe PAH and CTEPH as rare, progressive conditions that can be life-threatening and may require patients to remain on therapy for life.
For CTEPH, the approved use specifically includes persistent or recurrent disease after surgical treatment as well as inoperable disease; the treatment aims to improve exercise capacity and WHO functional class.
MSN founder and CMD Dr. MSN Reddy called riociguat a technically demanding molecule and said the partnership aims to deliver a consistent, high-quality supply.
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