Veletri Injection, Powder, Lyophilized, For Solution
Product Images NDC 66215-403

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Veletri (NDC 66215-403). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actelion Pharmaceuticals Us, Inc., 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

Chemical Structure (Veletri 01)

Chemical structure diagram of epoprostenol showing its molecular backbone with various functional groups, including hydroxyl and carboxylate groups, as part of the active ingredient structure in Veletri injection.*

FDA Label Image

Principal Display Panel (0.5 mg Vial Carton)

Packaging label for Veletri (epoprostenol) injection, powder, lyophilized, for solution, 0.5 mg (500,000 ng) per vial. The label states it is a sterile lyophilized product for intravenous infusion only, manufactured for Actelion Pharmaceuticals US, Inc., a Janssen Pharmaceutical Company. The label includes storage instructions and notes to see full prescribing information. The label also features the Janssen logo and barcodes.*

FDA Label Image

Principal Display Panel (1.5 mg Vial Carton)

Veletri 1.5 mg (1,500,000 ng) vial label for epoprostenol injection, lyophilized powder for intravenous infusion. The label includes storage instructions, dosage reference to full prescribing info, and states it is a sterile product. The labeler is Actelion Pharmaceuticals US, Inc., a Janssen company, with manufacturing in the Czech Republic.*

* 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.