Epoprostenol Injection, Powder, Lyophilized, For Solution
Product Images NDC 67457-587

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Epoprostenol (NDC 67457-587). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Epoprostenol For Injection 0.5 mg Carton Label (Image 01)

Epoprostenol For Injection 0.5 mg Carton Label (Image 01)
Packaging label for Epoprostenol 0.5 mg (500,000 ng) vial, injection powder, lyophilized for intravenous infusion only. Manufactured by Mylan Institutional LLC. Label includes dosage form, strength, storage instructions, and single-dose vial designation with Mylan logo.*
FDA Label Image

Epoprostenol For Injection 1.5 mg Carton Label (Image 02)

Epoprostenol For Injection 1.5 mg Carton Label (Image 02)
Packaging label for Epoprostenol for Injection, 1.5 mg (1,500,000 ng)/vial, a sterile, lyophilized powder for intravenous infusion. The label shows it is a single-dose vial, manufactured for Mylan Institutional LLC. Storage instructions and contents are listed, emphasizing careful handling and discard of unused portions.*
FDA Label Image

Infusion Rate Formula (Image 03)

Infusion Rate Formula (Image 03)
An instructional formula diagram showing how to calculate the infusion rate in mL per hour. The formula divides the product of dose (ng/kg/min), weight (kg), and 60 minutes per hour by the final concentration (ng/mL).*
FDA Label Image

Epoprostenol Structural Formula (Image 04)

Epoprostenol Structural Formula (Image 04)
Chemical structure diagram of the active ingredient Epoprostenol, showing the molecular arrangement including sodium salt, carboxyl, hydroxyl, and hydrocarbon groups.*

* 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.