Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 76420-671

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 76420-671). 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

Pantoprazole20mg (Pantoprazole20mg)

Pantoprazole20mg (Pantoprazole20mg)
Labels for Pantoprazole Sodium DR Tablets, USP 20 mg by Enovachem Pharmaceuticals. Multiple configurations shown with quantities of 10, 30, 60, and 100 tablets. Each label includes NDC numbers, packaging details, warnings about prescription dispensing, storage instructions, and manufacturer information for Camber Pharmaceuticals, Inc., Torrance, CA.*
FDA Label Image

Pantoprazole40mg (Pantoprazole40mg)

Pantoprazole40mg (Pantoprazole40mg)
Packaging labels for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, from Enovachem Pharmaceuticals. Labels show different package sizes including quantities of 10, 30, 60, 90, and 100 tablets. Manufactured for Camber Pharmaceuticals, Inc., these labels include NDC numbers, storage and caution information, and batch/lot placeholders. The tablets are yellow to pale yellow, oval, delayed-release, and debossed as described.*
FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure of pantoprazole sodium, showing the molecular arrangement including fluorine atoms, sodium ion, methoxy groups, and hydration 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.