FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 63629-2014 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA075805
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20010416
Package count1

External sources

Source: openFDA. Public-domain (CC0).