Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 60760-679

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 60760-679). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

679 (Pantoprazole 60760 679 30)

679 (Pantoprazole 60760 679 30)
Label for Pantoprazole Sodium Delayed-Release Tablets USP 40 mg, 30 count, prescription drug. The label includes NDC 60760-679-30, manufacturer St. Mary's Medical Park Pharmacy in Oro Valley, AZ, and mentions storage at controlled room temperature 15°-30°C (59°-86°F). Additional details include lot number and expiration placeholders and a QR code.*
FDA Label Image

Camberlogo1 (Camberlogo1)

FDA Label Image

Camberlogo2 (Camberlogo2)

FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure of pantoprazole shown as a molecular diagram including fluorine atoms, sodium ion, and methoxy groups, consistent with the active ingredient pantoprazole sodium in the product.*

* 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.