FDA NDC Directory · JSON-LD · Markdown

SILDENAFIL

NDC 52817-341 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesildenafil
Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204882
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (50 mg/1)
Marketing started20180701
Package count2

External sources

Source: openFDA. Public-domain (CC0).