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Famotidine

NDC 55111-396 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerDr.Reddys Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077367
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20060930
Package count10

External sources

Source: openFDA. Public-domain (CC0).