Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51079-051

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 51079-051). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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.

FDA Label Image

Pantoprazole Structural Formula (8f0bbcb2 8643 41a9 B9fd A5f25a7dba5d 01)

FDA Label Image

Pantoprazole Sodium Delayed-release 40 mg Tablets Unit Carton Label (Image 01)

Pantoprazole Sodium Delayed-release 40 mg Tablets Unit Carton Label (Image 01)
This is a description of Pantoprazole Sodium Delayed-Release Tablets, USP. The NDC number is 51079-051-20 and they come in a pack of 100 tablets. The tablets should be swallowed whole and should not be split, chewed, or crushed. The recommended dosage should be determined by a physician. The tablets should be stored at room temperature (20°-28°C or 68°-77°F). The manufacturer is Mylan Pharmaceuticals Inc. and their address is in Morgantown, WI.*
FDA Label Image

Unit Carton (Image 02)

Unit Carton (Image 02)
This is a packaging disclaimer for a drug manufactured by Mylan®. The package is not child resistant and should be kept out of reach of children. The container provides light-resistance and the package includes a window for the lot number and expiration date. This drug is intended for institutional use only.*

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