Zantac 360 Tablet, Film Coated
Product Images NDC 85237-1926

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Zantac 360 (NDC 85237-1926). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Select Consumer Group Llc, 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

Zantac360-1 (2411926008 Zantac 360 1926 1)

Packaging label for Zantac 360 Maximum Strength, film-coated tablet containing Famotidine USP 20 mg. The front shows a single tablet pack with the product name and strength prominently displayed, highlighting its use as an acid reducer that prevents and relieves heartburn. The back panel includes detailed Drug Facts, ingredient list, usage directions, warnings, and manufacturer information, Select Consumer Group LLC.*

FDA Label Image

Zantac360-2 (2421926008 Zantac 360 1926 2)

Packaging label for Zantac 360, maximum strength famotidine 20 mg oral film-coated tablets. The front panel shows a 2-tablet multi-pack with text highlighting prevention and relief of heartburn due to acid indigestion. The back panel displays drug facts including active ingredient, uses, warnings, directions, and inactive ingredients. Manufactured for Chattem, Inc. and repackaged by Select Consumer Group LLC.*

* 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.