Naltrexone Hydrochloride Tablet, Film Coated
Product Images NDC 70518-2718

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Naltrexone Hydrochloride (NDC 70518-2718). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Naltrexone HCl 50mg 70518 2718 00

Naltrexone Hydrochloride 50 mg film-coated tablets, package quantity 30, labeled as prescription only. The label includes NDC 70518-2718-00, manufacturer Sun Pharma, and repackager RemedyRepack Inc. with storage instructions and a notice to keep out of the reach of children.*

FDA Label Image

Naltrexone HCl 50mg 70518 2718 01

Label for Naltrexone HCl 50 mg film-coated tablets, quantity 28. The label includes NDC 70518-2718-01 and states the product is repackaged by Remedy Repack Inc. It notes manufacturing by Sun Pharma, Cranbury, NJ. Directions indicate to see package insert and storage instructions are provided.*

FDA Label Image

Naltrexone-structure (Naltrexone Structure)

Chemical structure of naltrexone hydrochloride, showing its molecular formula C20H23NO4·HCl and molecular weight 377.6.*

* 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.