# FENOFIBRIC ACID DELAYED-RELEASE

NDC: 42385-945
Generic name: Fenofibric Acid
Labeler / Manufacturer: Laurus Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200824

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:"42385-945"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42385-945
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=302ffbf8-448e-4729-949f-40d457e30ab4