Hydromorphone Hydrochloride Injection, Solution
Product Images NDC 0641-6254

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 0641-6254). 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.

FDA Label Image

Structural Formula (Hydromorphone Hydrochloride Injection Usp Nda 1)

Chemical structure diagram of Hydromorphone Hydrochloride, depicting the molecular rings and functional groups including hydroxyl, ketone, and methylamine moieties, along with a hydrochloride (HCl) component.*

FDA Label Image

Hydromorphone 20 mL Mdv Label (Hydromorphone Hydrochloride Injection Usp Nda 2)

Label for Hydromorphone Hydrochloride Injection 2 mg/mL, 40 mg per 20 mL multiple-dose vial by Hikma Pharmaceuticals USA Inc. The label indicates use for subcutaneous, intramuscular, or slow intravenous administration, with storage instructions and dosage information references included.*

FDA Label Image

Hydromorphone 20 mL Mdv Carton (Hydromorphone Hydrochloride Injection Usp Nda 3)

Carton label for Hydromorphone Hydrochloride Injection 2 mg/mL (40 mg per 20 mL) by Hikma Pharmaceuticals USA Inc. The label specifies use for subcutaneous, intramuscular, or slow intravenous administration. It includes storage instructions, ingredients, and dosage form details, along with multiple barcodes and regulatory information.*

* 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.