# Niacin

NDC: 65162-322
Generic name: Niacin
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20151211

FDA application: ANDA204178

## Active ingredients

- NIACIN: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7250313b-b2ef-4736-bd25-2f29c2ac0eb9