# Fenofibrate

NDC: 42858-067
Generic name: Fenofibrate
Labeler / Manufacturer: Rhodes Pharmaceuticals L.P.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170601

FDA application: ANDA075753

## Active ingredients

- FENOFIBRATE: 67 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42858-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42858-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=829f5c2e-3329-4644-bccb-267afb678540