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Famotidine 20 mg

NDC 25000-124 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerMARKSANS PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA217543
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20250523
Package count3

External sources

Source: openFDA. Public-domain (CC0).