# Niacin

NDC: 70752-295
Generic name: Niacin
Labeler / Manufacturer: QUAGEN PHARMACEUTICALS LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260806

FDA application: ANDA203899

## 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:"70752-295"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70752-295
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=249e27ac-e1e7-42dc-84f6-cd32fd1d9dee