FDA NDC Directory · JSON-LD · Markdown

signature care acid controller

NDC 21130-249 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerSafeway
Marketing categoryAbbreviated NDA (generic) · App ANDA075400
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (10 mg/1)
Marketing started20150904
Package count1

External sources

Source: openFDA. Public-domain (CC0).