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Finasteride

NDC 47335-714 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090508
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (1 mg/1)
Marketing started20221123
Package count5

External sources

Source: openFDA. Public-domain (CC0).