Sucralfate Tablet
Product Images NDC 70518-3959

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 70518-3959). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Figure (50be7e37 3381 49ff Afe2 Ca6a50245bf8 01)

Figure (50be7e37 3381 49ff Afe2 Ca6a50245bf8 01)
Not available*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Sucralfate is a medication available in tablet form. This particular package contains 30 tablets. The medication is only available with a prescription (RX ONLY). The National Drug Code (NDC) for this product is 70518-3958-00. The lot number and expiration date are not provided in the text. The source NDC is 72578-0081-01. The manufacturer is Viena Pharmaceuticals Inc, based in Cranford, NJ 07016. It is important to keep this medication out of the reach of children. The text also mentions that the directions for use can be found in the package insert. The storage temperature should be between 20-25°C (58-77°F), with excursions permitted up to 15-30°C (59-86°F) according to USP guidelines. The medication has been repackaged by RemedyRepack Inc. who are based in Indiana, PA 15701.*

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