Pantoprazole Tablet, Delayed Release
Product Images NDC 67046-0789

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pantoprazole (NDC 67046-0789). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coupler 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

Label (55111 332 90 Pantoprazole 20mg 67046 789 30)

Pantoprazole Sodium delayed-release tablets, 20 mg, label shows product strength, pill ID R332, and packaging by Coupler LLC. The label includes barcodes, lot number, expiration date, storage instructions at 25°C with permitted excursions, and states each tablet contains 20 mg pantoprazole equivalent. Marked RX only and includes usual dosage information reference.*

* 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.