Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 72865-229

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 72865-229). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xlcare Pharmaceuticals 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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This is a description for a medication with the NDC number 72865-229-90. The medication is Pantoprazole Sodium with a delayed-release formulation in the form of USP tablets called Delaxed-Release. The medication is available by prescription only and comes with 90 tablets. Unfortunately, the remaining text is not legible.*
FDA Label Image

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FDA Label Image

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XLcare Pharmaceuticals Inc. offers delayed-release Pantoprazole Sodium tablets, each containing 40mg Pantoprazole sodium sesquihydrate USP (equivalent to Pantoprazole). The tablets are enteric-coated and must not be crushed, chewed, or split before administration. Store at temperatures between 20°C-25°C (68°F-77°F) as per USP Controlled Room Temperature. The medication guide must be dispensed to each patient along with 1000 tablets. To find the full prescribing information, refer to the package insert. For any queries, contact 1.866-495-1995. XLCare Pharmaceuticals Inc., located in Lawrenceville, GA, manufactures these tablets, while Evarc Pharmaceuticals in Hauppauge, NY, manufactures them for XLCare Pharmaceuticals.*
FDA Label Image

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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.