FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 21130-039 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerBetter Living Brands LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206531
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (10 mg/1)
Marketing started20230908
Package count2

External sources

Source: openFDA. Public-domain (CC0).