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Famotidine

NDC 70756-052 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLifestar Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075302
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20231019
Package count2

External sources

Source: openFDA. Public-domain (CC0).