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Famotidine

NDC 0527-5190 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217982
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20250602
Package count1

External sources

Source: openFDA. Public-domain (CC0).