# fenofibrate

NDC: 55700-876
Generic name: fenofibrate
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200721
Marketing ended: 20270630
FDA application: ANDA210138

## Active ingredients

- FENOFIBRATE: 160 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-876"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-876
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1fb3b66-cac9-49cd-a9f8-c4ce960f66e7