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Ezetimibe

NDC 69238-1154 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208803
Dosage form / routeTABLET · ORAL
Active ingredientsEZETIMIBE (10 mg/1)
Marketing started20170612
Package count4

External sources

Source: openFDA. Public-domain (CC0).