Naltrexone Hydrochloride Tablet, Film Coated
Product Images NDC 64850-300

View Photos of 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 Naltrexone Hydrochloride (NDC 64850-300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elite Laboratories, 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)

Chemical Structure (Naltrexone 01)
Chemical structure diagram of naltrexone hydrochloride, showing the arrangement of atoms and bonds representing the active ingredient in the drug product.*
FDA Label Image

Naltrexone Bottle Label 50 mg, 100 Count (Naltrexone HCl 100count)

Naltrexone Bottle Label 50 mg, 100 Count (Naltrexone HCl 100count)
Label for Naltrexone Hydrochloride Tablets, USP 50 mg, film-coated tablets. The label includes storage instructions, usual dosage directions referring to the package insert, and a caution to keep medications out of reach of children. Manufactured by Elite Laboratories, Inc., Northvale, NJ. The label also displays the NDC 64850-300-01 and a barcode. Package contains 100 tablets.*
FDA Label Image

Naltrexone Bottle Label 50 mg 30count (Naltrexone HCl 30count)

Naltrexone Bottle Label 50 mg 30count (Naltrexone HCl 30count)
Naltrexone Hydrochloride Tablets, USP 50 mg film-coated tablet label from Elite Laboratories, Inc. The label includes storage instructions, dosage advisory, and packaging information. It states 30 tablets per container, specifies child-resistant packaging, and displays the NDC 64850-300-30 barcode. The label also advises keeping medication out of children's reach.*

* 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.