Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 76420-806

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 76420-806). 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

Package Label-principal Display Panel (20 mg)

This image shows multiple packaging labels for Pantoprazole Sodium delayed release tablets USP 20 mg by Enovachem Pharmaceuticals. The labels indicate packaging for quantities of 10, 30, 60, and 90 tablets, with distribution by Aurobindo Pharma USA, Inc. Each label includes barcodes, NDC numbers, storage instructions to keep at controlled room temperature, and prescription-only status warnings.*

FDA Label Image

Package Label-principal Display Panel (40 mg)

Pantoprazole Sodium DR Tablets, USP 40 mg, packaging labels from Enovachem Pharmaceuticals located in Torrance, CA. Labels show NDC codes for quantities of 10, 30, 60, and 90 tablets, distributed by Aurobindo Pharma USA, Inc. The tablets are described as yellow, oval-shaped, coated, and debossed. Labels include storage and dispensing cautions and contain barcodes and QR codes.*

FDA Label Image

Chemical Structure (Pantoprazole Str)

Chemical structure of pantoprazole sodium showing its molecular arrangement, including aromatic rings, sulfur-oxygen, and sodium ion components, along with an indication of 1.5 hydrate water molecules (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.