Strength
500 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00480012649
Classification
Generic
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
ICOSAPENT ETHYLApproval Type
Generic (ANDA)
FDA Application
ANDA209525On Market Since
9/9/2022
Related Drugs
Same classification
No related drugs found.