Hydromorphone Hydrochloride Injection
Product Images NDC 0641-6151

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 0641-6151). 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

Structure (Hydromorphone Hydrochloride Injection Usp Anda 1)

Chemical structure of Hydromorphone Hydrochloride, showing its molecular framework including a phenolic hydroxyl group, ketone group, and the methylated nitrogen in the morphinan core, paired with hydrochloride (HCl).*

FDA Label Image

462-584-00 (Hydromorphone Hydrochloride Injection Usp Anda 2)

Label for Hydromorphone Hydrochloride Injection, USP, 2 mg/mL single dose vial. The label indicates the product is for subcutaneous, intramuscular, or slow intravenous use, with protection from light advised. It is manufactured by Hikma Pharmaceuticals USA Inc. The label includes the NDC 0641-6151-01 and barcodes for tracking.*

FDA Label Image

462-585-00 (Hydromorphone Hydrochloride Injection Usp Anda 3)

Label for Hydromorphone Hydrochloride Injection USP 2 mg/mL by Hikma Pharmaceuticals USA Inc. The label indicates the drug is for subcutaneous, intramuscular, or slow intravenous use only. It comes in 25 single-dose vials, each 1 mL. The NDC is 0641-6151-25. Instructions include storage at controlled room temperature and protection from light, with warnings not to use intrathecally or epidurally.*

FDA Label Image

Layout 1 (Hydromorphone Hydrochloride Injection Usp Anda 4)

Packaging label of Hydromorphone Hydrochloride injection 2 mg/mL by Hikma Pharmaceuticals USA Inc. The label includes a GTIN barcode, serial number, expiration date placeholder, and lot number placeholder.*

* 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.