United States · FDA National Drug Code directory

Icosapent

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63629-9312_9a7d5eb6-95f1-4c0e-b51f-6b79ba2e3971
Product NDC
63629-9312
Form
CAPSULE
Composition / generic term
Icosapent Ethyl
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20210621 / 20270930

Source-listed ingredients

  • ICOSAPENT ETHYL — 1000 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 120 CAPSULE in 1 BOTTLE (63629-9312-1) · 63629-9312-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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