# FENOFIBRATE

NDC: 51655-009
Generic name: FENOFIBRATE
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140507

FDA application: ANDA076509

## Active ingredients

- FENOFIBRATE: 160 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4b4447a1-8136-4258-b2c8-c5f9c1bcec92