FDA NDC Directory · JSON-LD · Markdown

Sildenafil

NDC 35561-252 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesildenafil
Labeler / ManufacturerBostal LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208494
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (50 mg/1)
Marketing started20200422
Package count2

External sources

Source: openFDA. Public-domain (CC0).