Naltrexone Hydrochloride Tablet, Film Coated
Product Images NDC 68084-291

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naltrexone Hydrochloride (NDC 68084-291). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

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Naltrexone hydrochloride 50 mg film-coated tablet, oral dosage form, beige oval-shaped with imprints '1170' on one side and scored with '5 | 0' on the other side. The image shows the tablet size against a millimeter scale. Product labeler is American Health Packaging.*

FDA Label Image

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Naltrexone Hydrochloride 50 mg film-coated tablets label by American Health Packaging. The label shows the dosage strength of 50 mg, packaging quantity of 30 tablets (3 x 10), and includes storage instructions, usage warnings, and distributor information from Columbus, Ohio. The product is identified as a prescription drug with NDC 68084-291.*

FDA Label Image

50 mg Naltrexone HCl Tablet Blister

Naltrexone Hydrochloride 50 mg film-coated tablet labels from American Health Packaging. Each label shows the drug name, strength, dosage form, and placeholders for lot number and expiration date. Barcodes appear along one edge for scanning.*

FDA Label Image

Naltrexone Structural Formula (A8e1e7e8 45ee 41de Af32 9a3f8332ca19 01)

Chemical structure of naltrexone hydrochloride, the active ingredient in NALTREXONE HYDROCHLORIDE 50 mg film-coated tablets by American Health Packaging. The image shows the molecular structure with the formula C20H23NO4 and hydrochloride (HCl) indicated, along with the molecular weight of 377.86.*

* 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.