Pantoprazole Sodium
Product Images NDC 70934-203

2 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 70934-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

Label (70934 203 90 Rev A 12 18)

Label (70934 203 90   Rev A 12 18)
Pantoprazole Sodium Delayed-Release Tablets USP 40 mg, package contains 90 tablets, labeled Rx only. The label includes storage instructions to keep between 15-30°C and out of reach of children. Repackaged by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label also shows the NDC 70934-203-90 and manufacturing details including MFG: 62175-617-43 and placeholders for lot number and expiration date.*
FDA Label Image

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)
Chemical structure of Pantoprazole Sodium as depicted in the image, showing a detailed molecular diagram including functional groups and the sodium ion, along with a hydration state of 1.5 water molecules.*

* 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.