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Cimetidine

NDC 51655-697 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecimetidine
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074246
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIMETIDINE (400 mg/1)
Marketing started20210401
Package count1

External sources

Source: openFDA. Public-domain (CC0).