FDA NDC Directory · JSON-LD · Markdown

Sildenafil

NDC 71205-088 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077342
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (100 mg/1)
Marketing started20171211
Package count6

External sources

Source: openFDA. Public-domain (CC0).