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Famotidine

NDC 51407-684 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075805
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20010416
Package count3

External sources

Source: openFDA. Public-domain (CC0).