Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 65862-559

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 65862-559). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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 (90 Tablets Bottle))

NDC 65862-559-90 is a prescription medication containing pantoprazole sodium in delayed-release tablet form (20 mg). The medication guide should be dispersed to each patient by the pharmacist. The tablets should not be split, chewed, or crushed before administration. The usual dosage is provided in accompanying information. The tablets should be stored in well-closed containers at a temperature between 20° and 25°C.*

FDA Label Image

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))

FDA Label Image

Package Label-principal Display Panel (40 mg (90 Tablets Bottle))

This is a description for Pantoprazole Sodium Delayed-Release Tablets, USP, which is a prescription medication. The tablets contain 40mg of pantoprazole sodium USP and should not be split, chewed, or crushed before administration. The medication guide needs to be dispensed separately by the pharmacist to each patient. The tablets are distributed by Aurobindo Pharma USA, Inc. and are stored at 20° to 25°C (68° to 77°F). The dosage information is provided separately. The code for the medication is TS/DRUGS/22/2009.*

FDA Label Image

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))

FDA Label Image

Chemical Structure (Pantoprazole Str)

* 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.