Naltrexone Hydrochloride Tablet, Film Coated
Product Images NDC 47335-326

2 FDA label images from Sun Pharmaceutical Industries, Inc. · 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 47335-326). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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-structure (Naltrexone Structure)

Naltrexone-structure (Naltrexone Structure)
Chemical structure of naltrexone hydrochloride showing its molecular formula C20H23NO4·HCl and molecular weight 377.46.*
FDA Label Image

Spl-naltrexone-label-50mg (Spl Naltrexone Label 50mg)

Spl-naltrexone-label-50mg (Spl Naltrexone Label 50mg)
Label for Naltrexone Hydrochloride Tablets, USP 50 mg, shown as film-coated tablets in a 30-count package. The label includes storage instructions (20° to 25°C with permitted excursions), dispensing directions to keep in a tight container, and states Rx only. Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ, and manufactured by Sun Pharmaceutical Industries Limited, India. The NDC is 47335-326-83.*

* 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.