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VARDENAFIL

NDC 70710-1069 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208960
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARDENAFIL HYDROCHLORIDE TRIHYDRATE (5 mg/1)
Marketing started20181101
Package count3

External sources

Source: openFDA. Public-domain (CC0).