Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 43353-027

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 43353-027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

40 mg 90 Count Bottle Label (43353 0027 60)

Pantoprazole Sodium DR 40 mg label for 90 tablets by Aphena Pharma Solutions - Tennessee, LLC. The white label includes active ingredient name, strength, quantity, storage instructions, manufacturer Kremers Urban Pharmaceuticals Inc., and repackager information. It indicates prescription use with barcodes on each side.*

FDA Label Image

20 mg 9000 Count Label (43353 0916 09)

Pantoprazole Sodium DR 20 mg label for 9000 tablets by Aphena Pharma Solutions - Tennessee, LLC. The label includes storage instructions and manufacturer information (Kremers Urban Pharmaceuticals Inc., Princeton, NJ). It is labeled for prescription use (RX Only).*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chemical Structure (Pantoprazole Sodium Delayed Release Tablets 1)

Chemical structure of pantoprazole sodium with 1.5 molecules of water, showing its aromatic rings, methoxy groups, sulfoxide, and sodium salt form.*

* 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.