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Famotidine

NDC 46122-735 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerisource Bergen
Marketing categoryAbbreviated NDA (generic) · App ANDA206531
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (10 mg/1)
Marketing started20230727
Package count2

External sources

Source: openFDA. Public-domain (CC0).