Pantoprazole Sodium Granule, Delayed Release
Product Images NDC 62756-071

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 62756-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-pantoprazole-carton (Spl Pantoprazole Carton)

Packaging label for Pantoprazole Sodium for Delayed-Release Oral Suspension 40 mg, containing 30 packets. The label indicates it is for oral use as a delayed-release granule suspension, with administration instructions for applesauce and apple juice. Distributed by Sun Pharmaceutical Industries, Inc., the label also features the NDC 62756-071-64 and manufacturer information from Sun Pharmaceutical Industries Limited, Mohali, India.*

FDA Label Image

Spl-pantoprazole-chemical-structure (Spl Pantoprazole Chemical Structure)

Chemical structure of pantoprazole sodium, showing the molecular arrangement including a substituted benzimidazole ring, sulfoxide group, and sodium salt form with hydration (1.5 H2O).*

FDA Label Image

Spl-pantoprazole-packet (Spl Pantoprazole Packet)

Label for Pantoprazole Sodium for Delayed-Release Oral Suspension, 40 mg, from Sun Pharmaceutical Industries, Inc. The label indicates the suspension is in apple juice or applesauce only and each packet contains 40 mg pantoprazole equivalent to 45.1 mg pantoprazole sodium USP (sesquihydrate). Storage temperature is 20° to 25°C (68° to 77°F). The label also includes the NDC 62756-071-60 and Rx only designation.*

* 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.