FDA NDC Directory · JSON-LD · Markdown

acid controller

NDC 37808-301 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA075400
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (10 mg/1)
Marketing started20151023
Package count2

External sources

Source: openFDA. Public-domain (CC0).