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)

This is a medication guide for the administration of Pantoprazole Sodium for Delayed-Release Oral Suspension in 40mg packets. It should not be crushed or chewed and must be taken 30 minutes before a meal. The medication can be administered by sprinkling intact granules on a teaspoon of applesauce, mixing with a small cup of apple juice, or via nasogastric tube administration. The carton contains child-resistant packets and should be stored between 20°C to 25°C. The medication guide can be accessed via the given website or from the pharmacist.*

FDA Label Image

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

FDA Label Image

Spl-pantoprazole-packet (Spl Pantoprazole Packet)

This is a description of a medication called Pantoprazole Sodium for Delayed-Release Oral Suspension. Each packet contains 40 mg of pantoprazole, which is equivalent to 45.1 mg of pantoprazole sodium USP (sesquihydrate). The medication is available in a suspension form that can be taken with either apple juice or applesauce. It is recommended to store the medication at a temperature between 20 to 25°C (68 to 77°F). The identification number for this medication is NDC 62756-071-60. This description is useful for people who need information about this medication.*

* 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.