FDA NDC Directory · JSON-LD · Markdown

FAMOTIDINE

NDC 72189-207 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufacturerdirect rx
Marketing categoryAbbreviated NDA (generic) · App ANDA075805
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20210603
Package count2

External sources

Source: openFDA. Public-domain (CC0).