Sucralfate Tablet
Product Images NDC 48433-091

View Photos of 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 48433-091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safecor Health 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

Sucralfate 1 Gram Tablets, Usp Unit Carton Label (Image 01)

Sucralfate 1 Gram Tablets, Usp Unit Carton Label (Image 01)
Sucralfate 1 gram tablets, USP, oral dosage form. The label indicates 100 tablets per package, with each tablet containing 1 gram of sucralfate. The labeler is Safecor Health LLC, and manufacturing is by Pliva Hrvatska d.o.o. in Croatia, with the product manufactured for Teva Pharmaceuticals USA, Inc. The label includes storage instructions and a tablet imprint '22 10' shown on a white tablet image.*
FDA Label Image

Unit Carton (Image 02)

Unit Carton (Image 02)
Packaging label for Sucralfate oral tablets, 1 g strength, from Safecor Health LLC. The label shows the UDL logo and includes storage and safety instructions such as that the unit dose package is not child resistant, is for institutional use only, and provides light resistance. The label also advises keeping the drug out of reach of children and checking the window for lot number and expiration date.*
FDA Label Image

Structural Formula For Sucralfate (Image 1)

Structural Formula For Sucralfate (Image 1)
Chemical structure of sucralfate, depicting its molecular arrangement with aluminum hydroxide and water molecules in variable amounts (x = 8 to 10 and y = 22 to 31). This schematic represents the active ingredient in the product.*

* 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.