Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 0378-6689

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 0378-6689). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan 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

Pantoprazole Structural Formula (8f0bbcb2 8643 41a9 B9fd A5f25a7dba5d 01)

Chemical structure of pantoprazole sodium showing its molecular framework including sodium ion, methoxy groups, sulfur dioxide group, and trifluoromethoxy side chain, consistent with the active ingredient in Pantoprazole Sodium tablets.*

FDA Label Image

Pantoprazole Sodium Delayed-release Tablets, Usp 20 mg Bottle Label (Image 01)

Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg, oral tablet, manufactured for Mylan Pharmaceuticals Inc. The label includes NDC 0378-6688-77 and specifies to swallow tablets whole. The package contains 90 tablets. It also shows storage instructions, dispensing notes, and a barcode with space for lot and expiration details.*

FDA Label Image

Pantoprazole Sodium Delayed-release Tablets, Usp 40 mg Bottle Label (Image 02)

Label for Pantoprazole Sodium Delayed-Release Tablets USP, 40 mg strength, manufactured for Mylan Pharmaceuticals Inc. The film-coated tablets are to be swallowed whole, with a package count of 90 tablets. The label includes dosage information, storage instructions, and barcodes, along with manufacturer details indicating the product is made in India.*

* 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.