Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 76420-669

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 76420-669). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

Pantoprazoledrtabletscontainer20mg (Pantoprazoledrtabletscontainer20mg)

Pantoprazoledrtabletscontainer20mg (Pantoprazoledrtabletscontainer20mg)
Packaging labels for Pantoprazole Sodium delayed-release tablets, USP 20 mg by Enovachem Pharmaceuticals. Labels display various package quantities: 10, 30, 60, and 90 tablets. They include NDC numbers and QR codes, manufacturer information (XLCare Pharmaceuticals, Inc.), and standard cautionary storage and dispensing notes.*
FDA Label Image

Pantoprazoledrtabletscontainer40mg1 (Pantoprazoledrtabletscontainer40mg)

Pantoprazoledrtabletscontainer40mg1 (Pantoprazoledrtabletscontainer40mg)
Four brown bottles with white labels of Pantoprazole Sodium DR Tablets, USP 40 mg, packaged by Enovachem Pharmaceuticals, located in Torrance, CA. Each label shows different quantities: 10, 30, 60, and 90 tablets. The labels feature a QR code, NDC 76420-669, barcodes, manufacturing details by XL Care Pharmaceuticals, and storage instructions at 20-25°C (68-77°F). Each bottle is identified as prescription-only (RX).*
FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure diagram of pantoprazole sodium, showing its molecular composition including fluorine atoms, sodium ion, and water of hydration (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.