Pantoprazole Tablet, Delayed Release
Product Images NDC 72603-178

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 (NDC 72603-178). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

Container1 (Container1)

Container1 (Container1)
Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg in a package containing 90 tablets. The label includes directions for pharmacists to dispense the medication guide to each patient, storage instructions, and manufacturer information for NorthStar Rx LLC and Dr. Reddy's Laboratories Limited. The label features a barcode and states the NDC code 72603-177-01.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg oral tablets, packaged in a 90-count container. The label includes dosing instructions, storage conditions, and manufacturer details, indicating NorthStar Rx LLC as the labeler and Dr. Reddy's Laboratories Limited as the manufacturer. The label also features a barcode and a pharmacist instruction to dispense the medication guide to each patient.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of pantoprazole sodium sesquihydrate, showing its molecular arrangement including aromatic rings, sulfoxide group, and sodium ion, consistent with the active ingredient pantoprazole.*

* 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.