Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 70518-0860

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 70518-0860). 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

Pantoprazole Sodium 40mg 70518 0860 01

Pantoprazole Sodium 40 mg delayed-release tablets in a quantity of 28. The label shows the product is RX only with NDC 70518-0860-01. It is repackaged by RemedyRepack Inc. and manufactured by Aurobindo Pharma, Dayton, NJ. Directions reference the package insert and storage instructions are included.*

FDA Label Image

Remedy_label (Remedy Label)

Pantoprazole Sodium 40 mg delayed-release tablets label. The label indicates a quantity of 90 tablets and includes manufacturer information of Aurobindo Pharma, Dayton, NJ. It shows the product is repackaged by RemedyRepack Inc., Indiana, PA, with storage instructions and a barcode.*

FDA Label Image

Chemical Structure (Pantoprazole Str)

Chemical structure diagram of pantoprazole sodium, showing its molecular framework with labeled functional groups and sodium ion, including a hydrate form indicated as 1.5 H2O.*

* 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.