Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51407-613

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 Pantoprazole Sodium (NDC 51407-613). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-612-90ol.jpg (51407 612 90ol)

51407-612-90ol.jpg (51407 612 90ol)
Pantoprazole Sodium delayed-release tablets label, USP 20 mg strength. The label states a package count of 90 tablets and includes the NDC 51407-612-90. It features instructions for pharmacists to dispense medication guides and storage conditions between 20°-25°C. Manufactured by Golden State Medical Supply, Inc.*
FDA Label Image

51407-613-90lb.jpg (51407 613 90lb)

51407-613-90lb.jpg (51407 613 90lb)
Pantoprazole Sodium 40 mg delayed-release tablets label showing a bottle containing 90 tablets. The label includes the National Drug Code (NDC) 51407-613-90, manufacturer information for Golden State Medical Supply, Inc., and storage instructions. It specifies that the product is for oral use and is prescription only (Rx only).*
FDA Label Image

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)
Chemical structure of pantoprazole sodium, depicted as a complex organic molecule including a pyridine ring with methoxy groups, a benzimidazole ring, and sulfoxide linkage, shown as a sodium salt hydrate form with 1.5 molecules of water.*

* 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.