Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 70010-191

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 70010-191). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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

Panto-dr-structure (Panto Dr Structure)

Chemical structure of pantoprazole sodium showing the molecular arrangement including a sulfoxide group, methoxy-substituted pyridine and benzimidazole rings, sodium ion, and associated water molecules (1.5 H2O).*

FDA Label Image

Pantoprazole-20mg-90s (Pantoprazole 20mg 90s)

Label panel for pantoprazole sodium delayed-release tablets, USP, 20 mg strength. The label includes dosage form as delayed-release tablets, quantity of 90 tablets, and notes that medication guides must be dispensed separately. Manufactured by Granules India Limited, distributed by Granules Pharmaceuticals Inc. Storage instructions and warnings against splitting or crushing tablets are visible. A QR code and barcode area for batch coding and serialization details are shown.*

FDA Label Image

Pantoprazole-40mg-90s (Pantoprazole 40mg 90s)

Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, oral tablets available in a package of 90 tablets. The label instructs swallowing tablets whole without splitting, chewing, or crushing. It includes storage conditions, a barcode, and manufacturer information for Granules India Limited, made for Granules Pharmaceuticals Inc., Chantilly, VA.*

* 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.