FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 67296-2133 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRedpharm Drug
Marketing categoryAbbreviated NDA (generic) · App ANDA075302
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20231019
Package count1

External sources

Source: openFDA. Public-domain (CC0).