Icosapent Ethyl Capsule
Product Images NDC 69238-2598

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Icosapent Ethyl (NDC 69238-2598). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image (9892d929 20d8 4461 Aa24 B992f8402345 01)

Image (9892d929 20d8 4461 Aa24 B992f8402345 01)
Chemical structure of Icosapent ethyl showing its molecular bonds and functional groups, including multiple double bonds and ester linkage.*
FDA Label Image

Icosapent Ethyl 1 Gm Label (9892d929 20d8 4461 Aa24 B992f8402345 02)

Icosapent Ethyl 1 Gm Label (9892d929 20d8 4461 Aa24 B992f8402345 02)
Label for Icosapent Ethyl Capsules 1 gram by Amneal Pharmaceuticals LLC. The label states each capsule contains 1 gram of icosapent ethyl. It shows packaging information for 120 capsules, with storage instructions and manufacturer details (Strides Pharma Science Ltd., India). The label includes barcodes and the NDC number 69238-2598-8.*
FDA Label Image

Icosapent Ethyl 0.5 G Label (9892d929 20d8 4461 Aa24 B992f8402345 03)

Icosapent Ethyl 0.5 G Label (9892d929 20d8 4461 Aa24 B992f8402345 03)
Icosapent Ethyl Capsules 0.5 gram label from Amneal Pharmaceuticals LLC. The label indicates prescription use with a count of 240 capsules. It shows storage instructions, manufacturer Strides Pharma Science Ltd., and barcode details. The label is primarily white with blue and black text and features the Amneal logo.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.