FDA NDC Directory · JSON-LD · Markdown

heartburn relief

NDC 41250-712 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namefamotidine
Labeler / ManufacturerMeijer Distribution Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20190417
Package count3

External sources

Source: openFDA. Public-domain (CC0).