Sufentanil Citrate
Product Images NDC 17478-050

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sufentanil Citrate (NDC 17478-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, 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 (Suf01 0006 01)

Chemical structure diagram showing the molecular formula of Sufentanil Citrate. The structure includes various functional groups and aromatic rings characteristic of the active ingredient Sufentanil.*

FDA Label Image

Principal Display Panel Text For Container Label (Suf01 0006 02)

Label for Sufentanil Citrate Injection, USP 50 mcg/mL in a 1 mL ampule. The label indicates it is preservative-free, intended for intravenous and epidural use. It is a prescription medication manufactured by Akorn, Inc. The NDC is 17478-050-01. Additional visible information includes a barcode and placeholders for lot and expiration dates.*

FDA Label Image

Principal Display Panel Text For Carton Label (Suf01 0006 03)

Packaging label for Sufentanil Citrate Injection, USP 50 mcg/mL by Akorn. The label indicates a box of 10 ampules, each containing 1 mL of the injection. It is preservative free, intended for intravenous and epidural use, and includes a warning about habit-forming potential. Storage instructions specify 20° to 25°C, protected from light. The label includes a barcode and the manufacturer's information for Akorn, Inc.*

* 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.