FDA NDC Directory · JSON-LD · Markdown

Cimetidine

NDC 69452-326 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecimetidine
Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218220
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIMETIDINE (800 mg/1)
Marketing started20250301
Package count2

External sources

Source: openFDA. Public-domain (CC0).