FDA NDC Directory · JSON-LD · Markdown

Acid Controller

NDC 37808-042 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20160914
Package count3

External sources

Source: openFDA. Public-domain (CC0).