FDA NDC Directory · JSON-LD · Markdown

SILDENAFIL CITRATE

NDC 71335-3111 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSILDENAFIL
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA091448
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (50 mg/1)
Marketing started20180611
Package count8

External sources

Source: openFDA. Public-domain (CC0).