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up and up famotidine

NDC 11673-061 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerTarget Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20120503
Marketing ended20260531
Package count1

External sources

Source: openFDA. Public-domain (CC0).