# Fenofibrate

NDC: 55111-395
Generic name: Fenofibrate
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20140407

FDA application: ANDA090859

## Active ingredients

- FENOFIBRATE: 130 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-395"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-395
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16ea8ce4-8c1c-4111-509e-86aa688d89a0