Pantoprazole Sodium Granule, Delayed Release
Product Images NDC 31722-032

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 31722-032). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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
FDA Label Image

Pantoprazoleoralsuspensioncartonlabel (Pantoprazoleoralsuspensioncartonlabel)

Pantoprazoleoralsuspensioncartonlabel (Pantoprazoleoralsuspensioncartonlabel)
Packaging label for Pantoprazole Sodium 40 mg delayed-release oral suspension packets. The label includes directions for suspension preparation, manufacturer information (Camber Pharmaceuticals, Inc.), and a barcode. The package contains 30 packets and indicates suspension in apple juice or applesauce only. Dimensions and color codes for print production are also shown.*
FDA Label Image

Pantoprazoleoralsuspensionfoillabel (Pantoprazoleoralsuspensionfoillabel)

Pantoprazoleoralsuspensionfoillabel (Pantoprazoleoralsuspensionfoillabel)
Label for Pantoprazole Sodium for Delayed-Release Oral Suspension, 40 mg, from Camber Pharmaceuticals, Inc. The label includes storage instructions, batch coding area, and barcode. The product is Rx only and intended for oral use.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of pantoprazole sodium showing the molecular arrangement, including fluorinated benzene, sulfoxide group, methoxy substituents, and sodium ion with hydrate.*

* 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.