Sucralfate Tablet
Product Images NDC 71335-2637

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 71335-2637). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl713352637)

Label for Sucralfate Tablets, USP 1 gram oral tablets. The label includes an NDC number 71335-2637-1, a quantity of 100 tablets, and indicates Rx only status. It states storage instructions from 20° to 25°C and dispensing requirements for a child-resistant container. The product is repackaged by Bryant Ranch Prepack, Inc., and manufactured by Greenstone LLC. The label also features barcodes and QR codes.*

FDA Label Image

Sucralfate Tablets Contain Sucralfate And Sucralfate Is An α-d-glucopyranoside, β-d-fructofuranosyl-, Octakis-(hydrogen Sulfate), Aluminum Complex. (Sucralfate 01)

Chemical structure diagram of sucralfate showing the molecular components and notation for its chemical groups, including the representation of hydroxyl groups and sulfate aluminum components.*

* 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.