Pantoprazole Sodium
Product Images NDC 63304-968

3 FDA label images from Ranbaxy Pharmaceuticals Inc. · 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 63304-968). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ranbaxy 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Image 01)

Structural Formula (Image 01)
Chemical structure of Pantoprazole Sodium showing the molecular arrangement including a sulfoxide group, methoxy substituents, and a fluorophenyl ring with sodium ion and a hydrate component (1.5 H2O).*
FDA Label Image

20 mg Label-90 Tablets (Image 02)

20 mg Label-90 Tablets (Image 02)
Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg tablet bottle label by Ranbaxy Pharmaceuticals Inc. The label includes NDC 63304-967-90 and states the product is for Rx only with 90 tablets per bottle. It instructs dispensing with the accompanying Medication Guide and lists storage conditions, usage warnings, and packaging details including a barcode and lot and expiration date areas.*
FDA Label Image

4o mg Label-90 Tablets (Image 03)

4o mg Label-90 Tablets (Image 03)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg tablet label from Ranbaxy Pharmaceuticals Inc. The label indicates a package of 90 tablets. It includes dosing instructions emphasizing tablets must not be split, crushed, or chewed, storage conditions between 20°-25°C, and notes for pharmacists to dispense the medication guide to each patient. Label also shows the NDC number and barcode.*

* 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.