Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 70518-1298

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 70518-1298). 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 1298 01

Pantoprazole Sodium 40mg 70518 1298 01
Pantoprazole Sodium 40 mg delayed-release tablets in a quantity of 100. The label shows the product is repackaged by RemedyRepack Inc. and manufactured by Aurobindo Pharma, Dayton, NJ. It includes directions to see the package insert and storage information, with a barcode and QR code present.*
FDA Label Image

Pantoprazole Sodium 40mg 70518 1298 02

Pantoprazole Sodium 40mg 70518 1298 02
Label for Pantoprazole Sodium 40 mg delayed-release tablet, quantity 1, repackaged by RemedyRepack Inc. The label shows NDC 70518-1298-02, manufacturer Aurobindo Pharma in Dayton, NJ, storage instructions, and a QR code.*
FDA Label Image

Pantoprazole Sodium 40mg 70518 1298 03

Pantoprazole Sodium 40mg 70518 1298 03
Pantoprazole Sodium 40 mg delayed-release tablets in a pack of 30. The label shows the drug name, dosage form, strength, and quantity. It is repackaged by RemedyRepack Inc., Indiana, with manufacturer listed as Aurobindo Pharma, Dayton, NJ. The label includes an NDC barcode, QR code, and storage instructions.*
FDA Label Image

Pantoprazole Sodium 40mg 70518 1298 04

Pantoprazole Sodium 40mg 70518 1298 04
Pantoprazole Sodium 40 mg delayed-release tablets in a quantity of 90. The label includes the Remedy Repack logo and states the product is prescription only. Manufacturer is Aurobindo Pharma, Dayton, NJ. The label advises storage conditions and repackaging by RemedyRepack Inc., Indiana, PA.*
FDA Label Image

Pantoprazole Sodium 40mg 70518 1298 05

Pantoprazole Sodium 40mg 70518 1298 05
Pantoprazole Sodium 40 mg delayed-release tablet label showing a quantity of 28 tablets. The label states it is prescription only with NDC 70518-1298-05. Manufactured by Aurobindo Pharma, Dayton, NJ, and repackaged by RemedyRepack Inc., Indiana, PA. Storage instructions and directions for use are included, with a QR code and barcode also visible.*
FDA Label Image

Pantoprazole Sodium 40mg 70518 1298 06

Pantoprazole Sodium 40mg 70518 1298 06
Pantoprazole Sodium delayed-release 40 mg tablet label showing quantity of 30 tablets. The label includes the NDC number 70518-1298-06, manufacturer Aurobindo Pharma Dayton NJ, and repackager RemedyRepack Inc. Packaging instructions and storage conditions are also present.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Pantoprazole Sodium 40 mg delayed-release tablets packaging label. The label indicates a quantity of 30 tablets. It is labeled as prescription only with NDC 70518-1298-00. The original manufacturer is Aurobindo Pharma, Dayton, NJ, and the medication is repackaged by RemedyRepack Inc. The label includes directions to see the package insert and storage instructions.*
FDA Label Image

Chemical Structure (Pantoprazole Str)

Chemical Structure (Pantoprazole Str)
Chemical structure of Pantoprazole Sodium showing its molecular configuration with associated sodium ion and water of hydration (1.5 H2O). The structure includes methoxy and difluoromethoxy functional groups and a sulfoxide moiety, characteristic of Pantoprazole Sodium.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.