Sucralfate Suspension
Product Images NDC 66689-305

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 66689-305). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vistapharm, 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 (Sucralfate 1)

FDA Label Image

Bottle Label (Sucralfate 2)

This is a description of an oral suspension medication containing sucralfate, which comes in a 10mL (2 teaspoons) bottle. Each bottle contains 1g of sucralfate. The recommended dosage for adults is 1g (2 teaspoons) four times a day, to be taken on an empty stomach. The medication should be shaken well before use and stored at controlled room temperature (20° to 25°C or 68° to 77°F). The manufacturer is VistaPharm, Inc. The package insert should be consulted for full prescribing information. The label includes a lot number and expiration date. Contact information for questions or comments is provided.*

FDA Label Image

Carton (Sucralfate 3)

This is a medication called Sucralfate in an oral suspension form. Each 10 mL of the suspension contains 1g of Sucralfate and the usual adult dosage is 2 teaspoons (10 mL) four times daily on an empty stomach. It is important to shake well before use and avoid freezing. The medication should be kept at room temperature (20° to 25°C or 68° to 77°F) and out of reach of children. The package insert should be consulted for full prescribing information. The text also includes two NDG numbers (00669-305-16 and 65669-305-18) which may refer to product codes.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.