FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 72189-543 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA075718
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20240313
Package count2

External sources

Source: openFDA. Public-domain (CC0).