FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 63187-129 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA075805
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20010416
Package count4

External sources

Source: openFDA. Public-domain (CC0).