Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51655-075

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 51655-075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 075 52)

Label (51655 075 52)
This is a description of a medication that contains Pantoprazole Sodium Delayed-Release Tablets, USP. Each tablet contains 20mg of pantoprazole. It is only available through prescription and comes in a container of 30 tablets. The product should be stored in the original container in a Controlled Room Temperature between 20°- 25°C (68°- 77°F). The medication must not be split, chewed, or crushed before administration. It is packaged by Northwind Pharmaceuticals and repackaged from Aurobindo Pharma USA, Inc under Lot 0000000000. The product is identified by the NDC number 51655-075-52 and the GTIN number 0035165075524.*
FDA Label Image

Chemical Structure (Pantoprazole Str)

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