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approval · primary record

MACITENTAN

FDA · NDA · 2025-04-02

AgencyFDA
Submission typeNDA
Action date2025-04-02
BrandOPSYNVI
SponsorACTELION
RouteORAL

Provenance

  • Source: openFDA Drugs@FDA
  • Fetched at: 2026-10-28T02:34:00.364Z
  • Licence class: public-domain
  • Verdict: primary-source
  • Entity id: FDA:MACITENTAN:2025-04-02

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MACITENTAN — approval | AEaH