Pantoprazole Sodium Injection, Powder, For Solution
Product Images NDC 71839-122
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 71839-122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Be 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.
Panto25scartonlabel (Panto25scartonlabel)
Pantocartonlabel (Pantocartonlabel)
Pantoprazole Sodium for Injection is a sterile, single-dose vial for intravenous infusion only, with a strength of 40 mg. Each vial contains 451 mg of pantoprazole sodium USP, equivalent to 40mg pantoprazole, and 1 mg edetate disodium. It requires reconstitution before use, with a usual dosage as stated in the package insert. It should be stored between 20° to 25°C, allowed excursions from 10° to 30°C, and protected from light. The unused portion should be discarded. Distributed by BE Pharmaceuticals in Cary, NC, and made in India. NDC 7183912201.*
Pantostr (Pantostr)
Pantoviallabel (Pantoviallabel)
This is a description for a prescription drug named Pantoprazole Sodium for Injection. Each vial of this medicine contains 45.1 mg of Pantoprazole. It is manufactured in India for BE Pharmaceuticals Inc. The drug needs to be reconstituted before administration. The usual recommended dosage is 40 mg per vial. It is advisable to read the package insert for dosage and administration details. The drug needs to be stored at a temperature range of 20° to 25°C (68° to 77°F) and protected from light. This medicine is for intravenous infusion only, and any unused portion should be discarded.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.