# Niacin

NDC: 71741-020
Generic name: Niacin
Labeler / Manufacturer: Redmont Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20000503

FDA application: ANDA040378

## Active ingredients

- NIACIN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71741-020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71741-020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f51f7e6d-b132-48d8-8bb1-54203472f0d8