Oxymorphone Hydrochloride Tablet
Product Images NDC 0054-0283

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 Oxymorphone Hydrochloride (NDC 0054-0283). 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

Chem

Chem
Chemical structure diagram of oxymorphone hydrochloride. The illustration shows the molecular framework including hydroxy groups, ketone groups, and a methylated nitrogen atom, representing the anatomical structure of oxymorphone hydrochloride.*
FDA Label Image

Label-10mg-tab-05.jpg (Label 10mg Tab 05)

Label-10mg-tab-05.jpg (Label 10mg Tab 05)
Label for Oxymorphone Hydrochloride Tablets USP 10 mg by West-Ward Pharmaceuticals Corp. The label includes storage instructions, dosage reference, and states the product contains 100 tablets. It also has a barcode and specifies the product is Rx only.*
FDA Label Image

Label-5mg-tab-05.jpg (Label 5mg Tab 05)

Label-5mg-tab-05.jpg (Label 5mg Tab 05)
Label for Oxymorphone Hydrochloride Tablets USP 5 mg by West-Ward Pharmaceuticals Corp, a Hikma company. The package contains 100 tablets. The label includes dosage strength, storage instructions (20° to 25°C), and a barcode. It states the tablets should be swallowed whole and are not to be broken, chewed, crushed, or dissolved.*

* 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.