Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51655-797

View Photos of 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 51655-797). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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 (51655 797 52 Master Bottle Label Approval Rev A 02 22)

Label (51655 797 52 Master Bottle Label Approval   Rev A 02 22)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, carton label showing 30 tablets. The label includes NDC 51655-797-52 and manufacturer Northwind Health Company, LLC. It states Rx only with storage instructions, warnings, and packaging details including serialization and lot information.*
FDA Label Image

Chemical Structure (Pantoprazole Str)

Chemical Structure (Pantoprazole Str)
Chemical structure of Pantoprazole Sodium showing its molecular components, including aromatic rings, sulfur, oxygen, nitrogen atoms, and sodium ion. The structure also depicts the hydrate form with 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.