Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51655-797

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 51655-797). 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 797 52 Master Bottle Label Approval Rev A 02 22)

Label (51655 797 52 Master Bottle Label Approval   Rev A 02 22)
This is a description of a medication called Pantoprazole Sodium, which comes in a delayed-release tablet form. The medication is available in a package size of 30 tablets and requires a prescription. The dosage instructions are mentioned on the package insert. The tablets cannot be split, chewed, or crushed before administration. The medication is to be stored in its original container at a controlled room temperature of 20° - 25°C. The medication contains Pantoprazole sodium USP, which is equivalent to 40mg of pantoprazole. The medication is repackaged by Northwind Pharmaceuticals and the lot number is 0000000000. It is essential to keep this medication out of the reach of children. The product has an expiration date of 00/00/0000.*
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.