# Fenofibrate

NDC: 43975-306
Generic name: Fenofibrate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180501

FDA application: ANDA209504

## Active ingredients

- FENOFIBRATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43975-306"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43975-306
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c740f57c-cac5-4526-a5a9-aaab65b1caf6