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Niacor

NDC 71740-001 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameNiacin
Labeler / ManufacturerAvondale Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040378
Dosage form / routeTABLET · ORAL
Active ingredientsNIACIN (500 mg/1)
Marketing started20000503
Package count1

External sources

Source: openFDA. Public-domain (CC0).