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Famotidine

NDC 83324-116 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerChain Drug Marketing Association INC
Marketing categoryAbbreviated NDA (generic) · App ANDA077367
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20201201
Package count2

External sources

Source: openFDA. Public-domain (CC0).