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Niacin

NDC 70752-296 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerQUAGEN PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203899
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIACIN (1000 mg/1)
Marketing started20260806
Package count1

External sources

Source: openFDA. Public-domain (CC0).