FDA NDC Directory · JSON-LD · Markdown

maximum strength

NDC 56062-194 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerPublix Super Markets Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20071203
Package count2

External sources

Source: openFDA. Public-domain (CC0).