# FENOFIBRIC ACID

NDC: 69315-282
Generic name: FENOFIBRIC ACID
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190718

FDA application: ANDA211626

## Active ingredients

- FENOFIBRIC ACID: 135 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=daa488be-f580-430c-a72c-80ac31bb3e40