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NIACIN

NDC 47335-613 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200484
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNIACIN (1000 mg/1)
Marketing started20140627
Package count5

External sources

Source: openFDA. Public-domain (CC0).