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Famotidine

NDC 64980-737 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerRISING PHARMA HOLDINGS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217655
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20260820
Package count1

External sources

Source: openFDA. Public-domain (CC0).