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Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 55154-7634
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 55154-7634). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Cardinal Health 107, 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.
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Pantoprazole Sodium Delayed-Release Tablets, USP are a prescription drug that comes in a pack of 10 tablets with each tablet containing 40mg of pantoprazole. The tablets are intended to be swallowed whole and not crushed, chewed or split. The dosage of the medicine should be taken as specified in the product packaging, which also contains necessary precautions and warnings. The packaging should be stored between 20° - 25 C (88" - 77 F) with excursions permitted 1015°-30° C (59° - 86° F) and a pharmacist should dispense medication with a medication guide. The product is manufactured in India and distributed in the USA by Major Pharmaceuticals and Cardinal Health. The package is not child-resistant and should be kept out of reach from children.*
* 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.
