FDA NDC Directory · JSON-LD · Markdown

Niacin

NDC 71741-020 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRedmont Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040378
Dosage form / routeTABLET · ORAL
Active ingredientsNIACIN (500 mg/1)
Marketing started20000503
Package count3

External sources

Source: openFDA. Public-domain (CC0).