Aurlumyn Injection, Solution
Product Images NDC 50633-340

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 Aurlumyn (NDC 50633-340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Btg International 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

Carton Label (Aurlumyn Carton Label Jpg 1mb)

Carton Label (Aurlumyn Carton Label Jpg 1mb)
AURLUMYN 100 mcg/mL injection packaging label for intravenous infusion. The label shows the proprietary name AURLUMYN with the generic name iloprost, emphasizing a 1 mL single-dose vial strength of 100 mcg/mL. It includes a NDC number 50633-340-01 and notes the product is for intravenous infusion only, must be diluted before use, and unused portions should be discarded. The label is branded by BTG International Inc and features the SERB Pharmaceuticals logo.*
FDA Label Image

Aurlumyn Vial Label (Aurlumyn Vial)

Aurlumyn Vial Label (Aurlumyn Vial)
AURLUMYN 100 mcg/mL (iloprost) injection label for intravenous infusion only. The label indicates a 1 mL single-dose vial with storage instructions at 20°C to 25°C (68°F to 77°F), and notes that the vial must be diluted before use. Manufactured by BTG International Inc, West Conshohocken, PA.*
FDA Label Image

Chemical Structure (Aurlumyn 01)

Chemical Structure (Aurlumyn 01)
Chemical structure diagram of iloprost, the active ingredient in AURLUMYN injection solution 100 mcg/mL by BTG International Inc. The structure shows key functional groups and stereochemistry characteristic of iloprost.*

* 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.