Pantoprazole Sodium
Product Images NDC 67296-1812

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 67296-1812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Epm Label (67296 1812 7)

Epm Label (67296 1812 7)
This is a description of a medication package of Pantoprazole Sodium DR, containing 14 tablets of 40mg. It includes the lot number, expiration date, and manufacturer's information (Mig: Aurobindo Pharma Limited, Hyderabad 500 038 India). The medication is Rx-only and should be stored at a controlled room temperature of 20-25 C (68-77 F). It is distributed by Redpharm Drug in Eden Prairie, MN 55344. The NDC number is 67296-1812-7, and the product is designated with a SIN number of 190085.*
FDA Label Image

Package Label-principal Display Panel (20 mg (90 Tablets Bottle))

Package Label-principal Display Panel (20 mg (90 Tablets Bottle))
NDC 65862-559-90 is a prescription-only medication containing Pantoprazole Sodium in the form of Delayed-Release Tablets. It is manufactured by Aurobindo Pharma USA, and each bottle of this medication comes with a medication guide. The tablets should not be chewed or crushed before administering, and they must be stored in a well-closed container at 68-77°F (20-25°C). The medication dosage information can be found in the accompanying information. *
FDA Label Image

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))

FDA Label Image

Package Label-principal Display Panel (40 mg (90 Tablets Bottle))

Package Label-principal Display Panel (40 mg (90 Tablets Bottle))
This is a description of a medication identified as NDC 65862-560-90 for the drug Pantoprazole Sodium. The medication is available in delayed-release tablet form to be dispensed only by a pharmacist. The tablets come in a bottle of 90 tablets, with each tablet containing pantoprazole 40 mg. The accompanying medication guide should be provided to each patient. The tablets should not be split, chewed, or crushed before use, and must be stored in a cool, dry place in a well-closed container. The medication was manufactured in India by Aurobindo and distributed by Aurobindo Pharma USA, Inc. Further dosage information is available in the accompanying information.*
FDA Label Image

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))

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.