# Fenofibric acid

NDC: 33342-295
Generic name: Fenofibric acid
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20240226

FDA application: ANDA207796

## Active ingredients

- CHOLINE FENOFIBRATE: 135 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-295"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-295
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af225492-73b0-49bb-b32f-5399c3c3ec6d