FDA NDC Directory · JSON-LD · Markdown

Sildenafil Citrate

NDC 52817-295 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSildenafil
Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204883
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (20 mg/1)
Marketing started20160801
Package count2

External sources

Source: openFDA. Public-domain (CC0).