Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 64980-676

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 64980-676). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

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Chemical structure of pantoprazole sodium sesquihydrate, showing its molecular composition including a substituted benzimidazole and sulfoxide group with sodium ion and 1.5 molecules of water of hydration.*

FDA Label Image

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Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg carton label showing a count of 90 tablets. The label includes dosing instructions, storage conditions, and manufacturer details. Manufactured by Graviti Pharmaceuticals Pvt. Ltd. in India and distributed by Rising Pharma Holdings, Inc.*

FDA Label Image

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Label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, oral dosage form. The label indicates 90 tablets, manufactured by Graviti Pharmaceuticals Pvt. Ltd., distributed by Rising Pharma Holdings, Inc. It includes storage instructions, dosage guidance to see accompanying information, and a barcode. The label also references a medication guide and lists Rx only.*

* 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.