FDA NDC Directory · JSON-LD · Markdown

Sildenafil

NDC 65862-690 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203962
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (50 mg/1)
Marketing started20180611
Package count4

External sources

Source: openFDA. Public-domain (CC0).