# ICOSAPENT ETHYL

NDC: 31722-299
Generic name: Icosapent ethyl
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240216

FDA application: ANDA216811

## Active ingredients

- ICOSAPENT ETHYL: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-299"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-299
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e3498ab-f35e-4597-8556-89bf9fdd1406