NDC 70710-1738 – Icosapent ethyl

Icosapent Ethyl .5 g/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC70710-1738

Product details

Brand name
Icosapent ethyl
Generic name
Icosapent ethyl
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA217656
Marketed since
August 4, 2023
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70710-1738-4240 CAPSULE in 1 BOTTLE (70710-1738-4)Aug 4, 2023

Recalls mentioning this NDC

Other Icosapent Ethyl products