Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 70518-0860

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 70518-0860). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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 Sodium 40mg 70518 0860 01

Pantoprazole Sodium is a delayed-release medication in tablet form, with a strength of 40 mg per tablet. It is only available with a prescription and has an National Drug Code (NDC) of 70518-0860-01. The medication should be stored at a temperature of 20-25°C (58-77°F), with excursions permitted to 15-30°C (59-86°F), and kept out of reach of children. The manufacturer of the medication is Aurobindo Pharma, located in Dayton, NJ. The medication was repackaged by RemedyRepack. Directions for use are listed in the package insert.*

FDA Label Image

Remedy_label (Remedy Label)

This is a bottle of 90 delayed-release Pantoprazole Sodium 40 mg tablets which expires but does not have a lot number listed. It also comes with directions for use in the package insert and should be stored between 20-25°C (58-77°F). The repackaging of this medication was done by RemedyRepack Inc. of Indiana, PA.*

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.