Sucralfate Tablet
Product Images NDC 71610-541

3 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 71610-541). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - 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

Bottle Label 1 Gram (71610 0541 60)

Bottle Label 1 Gram (71610 0541 60)
Label for Sucralfate USP 1 gram oral tablets, containing 90 tablets per bottle. Label indicates storage instructions between 20-25 degrees Celsius and dispensing in a tight light-resistant container. Manufactured by Nostrum Laboratories Inc., Kansas City, MO, and packed by Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN. Label includes NDC 71610-054-60 and notes RX only.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

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

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 its polymeric aluminum hydroxide complex with a sucrose sulfate backbone. The diagram includes notation for variable x and y indicating ranges for aluminum hydroxide and water components respectively, and the molecular formula for the sulfate-aluminum complex.*

* 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.