Sucralfate Tablet
Product Images NDC 80425-0091

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 80425-0091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Structure

Chemical structure diagram showing a molecular formula with multiple cyclic ether groups and hydroxyl (OH) groups, representing the active ingredient sucralfate, including notation for aluminum hydroxide and water components with variable x and y values.*

FDA Label Image

Sucralfate 1g Tab Qty 30 Ndc 80425 0091

Label for Sucralfate 1 G tablet, an oral human prescription drug by Advanced Rx of Tennessee, LLC, Nashville, TN. The label references NDC 80425-0091-01 and includes a lot number, expiration date, barcode, and storage instructions (store at room temperature 20°-25°C). The product is compared to Carafate and made by Teva USA.*

* 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.