Sucralfate Tablet
Product Images NDC 60219-1656

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 60219-1656). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

1 (Sucralfate Tablets Usp 1)

1 (Sucralfate Tablets Usp 1)
Chemical structure diagram of sucralfate showing its molecular components including a polysaccharide backbone with various hydroxyl groups and aluminum hydroxide sulfate (SO3Al(OH)2) substituents. The structure includes notation for variable hydration and aluminum hydroxide content.*
FDA Label Image

2 (Sucralfate Tablets Usp 2)

2 (Sucralfate Tablets Usp 2)
Label for Sucralfate Tablets, USP 1 gram oral tablets, containing 100 tablets per container. The label includes storage instructions, warnings, dispensing information, and manufacturer details for Amneal Pharmaceuticals NY LLC. A portion of the tablet with imprint A56 is also visible.*
FDA Label Image

1 (Sucralfate Tablets Usp 3)

1 (Sucralfate Tablets Usp 3)
Sucralfate Tablets USP 1 gram oral tablets label from Amneal Pharmaceuticals NY LLC. The label shows the product name, dosage strength of 1 gram, packaging of 500 tablets, and includes storage instructions, warnings, manufacturer and distributor information, and a barcode. The label also displays an image of a single pink oblong tablet embossed with 'A 56.'*

* 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.