Alprostadil Injection, Solution, Concentrate
Product Images NDC 71288-206

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 Alprostadil (NDC 71288-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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

Package Display Panel Alprostadil Injection, Usp 500 Mcg Per mL Carton (Alprostadil Carton)

Package Display Panel Alprostadil Injection, Usp 500 Mcg Per mL Carton (Alprostadil Carton)
Packaging label for Alprostadil injection, USP 500 mcg per mL, supplied as 10 single-dose 1 mL vials. The label indicates the drug is for intravenous use only and must be diluted before use. Manufactured by Meitheal Pharmaceuticals Inc., with storage instructions between 2°C and 8°C. The container closure does not contain natural rubber latex.*
FDA Label Image

Structure (Alprostadil Structure)

Structure (Alprostadil Structure)
Chemical structure of alprostadil, depicting its molecular arrangement including hydroxyl groups, carbonyl groups, and the linear carbon chain characteristic of the molecule.*
FDA Label Image

Package Display Panel Alprostadil Injection, Usp 500 Mcg Per mL Vial Label (Alprostadil Vial)

Package Display Panel Alprostadil Injection, Usp 500 Mcg Per mL Vial Label (Alprostadil Vial)
Label for Alprostadil Injection, USP, 500 mcg per mL, in a 1 mL single-dose vial for intravenous use. The product is manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, and is labeled to be stored refrigerated between 2° to 8°C. The label includes the NDC 71288-206-01 and a barcode.*

* 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.