FDA NDC Directory · JSON-LD · Markdown

Sildenafil Citrate

NDC 71205-305 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSildenafil
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA204883
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (20 mg/1)
Marketing started20190101
Package count5

External sources

Source: openFDA. Public-domain (CC0).