FDA NDC Directory · JSON-LD · Markdown

Major Heartburn Relief Maximum Strength

NDC 0904-5780 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20060929
Package count2

External sources

Source: openFDA. Public-domain (CC0).