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Famotidine

NDC 37835-165 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerBi-Mart
Marketing categoryAbbreviated NDA (generic) · App ANDA215822
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20250601
Package count1

External sources

Source: openFDA. Public-domain (CC0).