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Riociguat

NDC 70710-2157 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA211135
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRIOCIGUAT (1 mg/1)
Marketing started20260918
Package count2

External sources

Source: openFDA. Public-domain (CC0).