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Famotidine

NDC 69367-401 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217669
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20240909
Package count1

External sources

Source: openFDA. Public-domain (CC0).