Pantoprazole Sodium Granule, Delayed Release
Product Images NDC 42799-952

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 42799-952). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Edenbridge Pharmaceuticals 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

Box (Pantoprazole Box)

Box (Pantoprazole Box)
Pantoprazole Sodium 40 mg delayed-release oral suspension granules packaging label by Edenbridge Pharmaceuticals LLC. The label indicates 30 packets per package, with storage and patient administration instructions. Manufactured by Dexcel Pharma Technologies Ltd., Israel, and distributed by Edenbridge Pharmaceuticals, Parsippany, NJ. NDC 42799-952-30 displayed along with barcode.*
FDA Label Image

Packet (Pantoprazole Packet)

Packet (Pantoprazole Packet)
Pantoprazole Sodium 40 mg granule, delayed release oral suspension label showing the proprietary and generic name, dosage strength, and instructions for opening. The label includes storage instructions, a barcode, the National Drug Code (NDC) 42799-952-01, and the labeler Edenbridge Pharmaceuticals LLC. It notes the medication is for prescription use only and specifies suspension in apple juice or applesauce.*
FDA Label Image

Structure (Pantoprazole)

Structure (Pantoprazole)
Chemical structure diagram of Pantoprazole Sodium showing the molecular arrangement including methoxy groups, sulfoxide, and the sodium ion with 1.5 molecules of water.*

* 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.