Hydromorphone Hydrochloride Injection
Product Images NDC 0641-2341

3 FDA label images from Hikma Pharmaceuticals Usa Inc. · 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 Hydromorphone Hydrochloride (NDC 0641-2341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Hydromorphone Hydrochloride Injection Usp 1)

Structural Formula (Hydromorphone Hydrochloride Injection Usp 1)
Chemical structure of Hydromorphone Hydrochloride showing the molecular arrangement including aromatic rings, hydroxyl groups, and the hydrochloride component indicated separately.*
FDA Label Image

Vial (Hydromorphone Hydrochloride Injection Usp 2)

Vial (Hydromorphone Hydrochloride Injection Usp 2)
Hydromorphone Hydrochloride Injection, USP 2 mg/mL (40 mg per 20 mL) multiple dose vial label by Hikma Pharmaceuticals USA Inc. The label indicates use for subcutaneous, intramuscular, or slow intravenous administration. It includes dosing details, storage instructions, and a volume scale on the left side of the label.*
FDA Label Image

Carton (Hydromorphone Hydrochloride Injection Usp 3)

Carton (Hydromorphone Hydrochloride Injection Usp 3)
Packaging label for Hydromorphone Hydrochloride Injection, USP 2 mg/mL (40 mg per 20 mL). This label set is for a 20 mL multiple dose vial for subcutaneous, intramuscular, or slow intravenous use. The product is manufactured by Hikma Pharmaceuticals USA Inc., with storage instructions and warnings included on the label.*

* 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.