# Icosapent

NDC: 43598-267
Generic name: Icosapent Ethyl
Labeler / Manufacturer: Dr. Reddy's Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210621

FDA application: ANDA209499

## Active ingredients

- ICOSAPENT ETHYL: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-267"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-267
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1aca884c-c464-900d-ac06-33aee7118df8