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Sildenafil Citrate

NDC 68071-3592 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSildenafil
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206401
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (25 mg/1)
Marketing started20181012
Package count2

External sources

Source: openFDA. Public-domain (CC0).