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Vardenafil Hydrochloride

NDC 71335-9688 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA091347
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARDENAFIL HYDROCHLORIDE (20 mg/1)
Marketing started20190103
Package count1

External sources

Source: openFDA. Public-domain (CC0).