Pantoprazole Sodium Injection, Powder, For Solution
Product Images NDC 55150-202

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 55150-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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.

FDA Label Image

Package Label-principal Display Panel (40 mg per vial)

Package Label-principal Display Panel (40 mg per vial)
Pantoprazole Sodium for Injection by Auromedics is a sterile single-dose vial containing 42.3 mg of pantoprazole sodium, USP equivalent to 40 mg of pantoprazole. The vial requires reconstitution before intravenous infusion. It also contains 1 mg edetate disodium and sodium hydroxide to adjust pH. The package insert should be consulted for dosage and administration information. The product should be protected from light and stored at 20° to 25°C. This product is manufactured by AuroMedics Pharma LLC in India.*
FDA Label Image

Package Label-principal Display Panel (40 mg per vial)

Package Label-principal Display Panel (40 mg per vial)
This text contains information about a pharmaceutical product called Pantoprazole Sodium, which is for injection purposes only. The vials contain 42.3 mg of pantoprazole and are sterile and single-dose. The product is distributed by AuroMedics Pharma LLC and should be stored in a controlled room temperature. No filter is required for the infusion. The text also includes a code: TSDRUGS/13/2010.*
FDA Label Image

Package Label-principal Display Panel (40 mg per vial)

Package Label-principal Display Panel (40 mg per vial)
This appears to be a product description for a medication called Pantoprazole Sodium for Injection, manufactured by a company called Auromedics Pharma LLC. It comes in a single-dose vial containing 42.3 mg of the active ingredient, Pantoprazole Sodium USP, which is equivalent to 40 mg of Pantoprazole, and requires reconstitution prior to use. The usual dosage is not provided, but can be found in the package insert. The medication is intended for intravenous infusion only and is stored at 20-25 degrees Celsius. The product is sterile and comes in a carton that should be kept until use, and no filter is required. There is a code of TSDRUGS/13/2010 N355150202256, however it is unclear what this code pertains to.*
FDA Label Image

Pantoprazole Sodium Chemical Structure (Pantoprazole Str)

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