FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 71335-2190 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA216441
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20220606
Package count9

External sources

Source: openFDA. Public-domain (CC0).