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Niacin

NDC 62175-320 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203899
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIACIN (500 mg/1)
Marketing started20170216
Package count2

External sources

Source: openFDA. Public-domain (CC0).