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Famotidine

NDC 0615-8559 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078916
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20160129
Package count2

External sources

Source: openFDA. Public-domain (CC0).