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Famotidine

NDC 49035-505 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerWal-Mart Stores, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206531
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20160426
Package count7

External sources

Source: openFDA. Public-domain (CC0).