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Niacin

NDC 65162-322 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204178
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNIACIN (750 mg/1)
Marketing started20151211
Package count3

External sources

Source: openFDA. Public-domain (CC0).