NDC 67184-0582 – Icosapent Ethyl

Icosapent Ethyl 1 g/1 · Capsule · Oral

Human Prescription Drug

Product NDC67184-0582

Product details

Brand name
Icosapent Ethyl
Generic name
Icosapent Ethyl
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA218899
Marketed since
January 1, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Icosapent Ethyl →

Package NDC codes (1)

Package NDCDescriptionSince
67184-0582-1120 CAPSULE in 1 BOTTLE (67184-0582-1)Jan 1, 2025

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