Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 72789-086

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 72789-086). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

72789086 Label (72789086)

This medicine is Pantoprazole Sodium DR USP, which is available in three containers of 30 tablets each with lot number F20A56 which expires on 09/2021. Each delayed-release tablet contains 40 mg of Pantoprazole. The tablets should not be crushed or chewed and should be taken as recommended by the doctor. The packaging insert should be checked for dosage and storage information. Children should be kept away from this medication. If any side effect occurs, inform your doctor or call FDA at 1-800-FDA-1088. There are organoleptic markings on the tablets. Other information such as GTIN, manufacturer and some unreadable text is also provided.*

FDA Label Image

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)

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