Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 62175-618

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 62175-618). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)

Chemical structure of Pantoprazole Sodium including its hydrate form (1.5 H2O), showing the molecular components and bonding.*

FDA Label Image

20 mg (Pantoprazole Sodium Delayed Release Tablets 2)

Pantoprazole Sodium Delayed-Release Tablets USP 20 mg label from Lannett Company, Inc. The label states the strength as 20 mg per tablet and indicates a container with 90 tablets. It includes usage information about dosage, storage conditions, and administration instructions. The label also features the Lannett logo and a barcode.*

FDA Label Image

40 mg (Pantoprazole Sodium Delayed Release Tablets 3)

Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg, packaged by Lannett Company, Inc. The label displays dosage strength 20 mg and specifies 90 tablets per container. It includes usage notes such as dispensing instructions for pharmacists and storage temperature guidelines. The label is primarily white with black and orange text elements.*

FDA Label Image

Pantoprazole Sodium Delayed Release Tablets 4

Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg label from Lannett Company, Inc. The label includes dosage strength, NDC code, quantity of 90 tablets, and storage instructions. It specifies the product is Rx only and provides a URL for medication guides.*

* 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.