Pantoprazole Sodium Injection, Powder, For Solution
Product Images NDC 72603-128

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 72603-128). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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.

Product Images & Figures Index

FDA Label Image

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Carton (Panto Ns Dl Carton)

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Carton (Panto Ns Dl Carton)
Packaging label for Pantoprazole Sodium for Injection 40 mg per vial, an intravenous infusion powder for solution. The label indicates the product contains 10 single-dose vials, is sterile, and manufactured for Northstar Rx LLC. The label includes storage instructions, barcode, and presentation QR code for product identification.*
FDA Label Image

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Vial Label (Panto Ns Dl Vial)

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Vial Label (Panto Ns Dl Vial)
Pantoprazole Sodium for Injection 40 mg per vial label for intravenous infusion. The sterile single-dose vial is labeled for use by Northstar Rx LLC, manufactured in China. It includes dosing instructions, storage conditions, barcode, and expiry date fields.*
FDA Label Image

Structural Formula (Panto Structure)

Structural Formula (Panto Structure)
Chemical structure of Pantoprazole Sodium, showing its molecular arrangement including benzene rings, sulfoxide group, sodium ion, and fluorinated substituents.*

* 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.