Naltrexone Hydrochloride Tablet, Film Coated
Product Images NDC 51224-206

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Naltrexone Hydrochloride (NDC 51224-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tagi Pharma 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

Chemical Structure (Naltrexone 01)

FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

Principal Display Panel (50 mg Tablet Bottle Label)
This is a package insert for Naltrexone Hydrochloride, an opioid antagonist medication used to manage alcohol and opioid dependence. The usual dosage is 50mg per film-coated tablet intended for adult use only. It should be stored at 20° to 25°C (68° to 77°F) and kept tightly closed. The package should be dispensed in a tight and light-resistant container that is child-resistant. Protect it from light and keep it out of the reach of children. The manufacturing company is Elite Laboratories, Inc. The drug is distributed by an unknown company with the NDC number 51224-206-50. The text includes cautionary instructions for adults to use only, storage conditions, and the labelling requirements for this medication.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.