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SILDENAFIL CITRATE

NDC 60290-003 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUmedica Laboratories USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209302
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (100 mg/1)
Marketing started20260215
Package count5

External sources

Source: openFDA. Public-domain (CC0).