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famotidine

NDC 83324-008 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerCHAIN DRUG MARKETING ASSOCIATION, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215766
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20240306
Package count1

External sources

Source: openFDA. Public-domain (CC0).