Hydromorphone Hydrochloride
Product Images NDC 0054-0265

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 0054-0265). 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

Hydromorphone-chem.jpg (Hydromorphone Chem)

Chemical structure of Hydromorphone Hydrochloride, showing a multi-ring structure with hydroxyl, ketone, and methylamine groups, along with the hydrochloride salt component.*

FDA Label Image

Image 01

Hydromorphone Hydrochloride 1 mg/mL oral solution label from Hikma Pharmaceuticals USA Inc. The label includes dosage strength, volume (473 mL), storage instructions, and distribution information. It prominently displays warnings and usage instructions, including habit-forming potential and shaking before use.*

FDA Label Image

Image 02

Label for Hydromorphone Hydrochloride tablets, USP, 4 mg strength. The label indicates a package size of 100 tablets and includes storage instructions. The product is distributed by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. The label features a barcode and note for prescription use only.*

FDA Label Image

Image 03

Hydromorphone Hydrochloride 8 mg Tablets, USP packaging label showing 100 tablets per container. The label includes dosage information, storage instructions at 20° to 25°C, and dispensing requirements. Distributed by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. The label clearly marks the product as Rx only and includes a barcode and NDC 0054-0265-25.*

* 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.