Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 48433-081

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 48433-081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safecor Health 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

Pantoprazole Sodium Structural Formula (Image 01)

FDA Label Image

Pantoprazole Sodium 40 mg Delayed-release Tablets, Usp Unit Carton Label (Image 02)

Pantoprazole Sodium 40 mg Delayed-release Tablets, Usp Unit Carton Label (Image 02)
This is a description for Pantoprazole Sodium Delayed-Release Tablets, USP with NDC 48433-081-20. The tablets should be swallowed whole and not split, chewed, or crushed. Each bottle contains 100 tablets (10x10) and requires a prescription.*
FDA Label Image

Unit Carton (Image 03)

Unit Carton (Image 03)
This is a package that is not resistant to high humidity. It is intended for institutional use. The container provides light resistance. It is suitable for the storage of KaspĀ® and alcohol wipes for easy reach. It can hold a specific number of wipes and has an expiration date window. Distributed by Safecor Health LLC in Rockford, IL, USA. Website: SafecorHealth.com. Contact number is 1-800-447-1006.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.