# FENOFIBRATE

NDC: 0115-5511
Generic name: FENOFIBRATE
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100201

FDA application: ANDA076509

## Active ingredients

- FENOFIBRATE: 54 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-5511"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-5511
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa08cf6a-d306-4979-9b23-ac7febf4fd12