Protonix Injection, Powder, For Solution
Product Images NDC 55154-4225

3 FDA label images from Cardinal Health 107, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Protonix (NDC 55154-4225). 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.

FDA Label Image

0e813403 54ba 4523 9123 592cd3232ade 00

0e813403 54ba 4523 9123 592cd3232ade 00
Label for Protonix I.V. (pantoprazole sodium) injection powder in 40 mg strength, supplied as 5 single dose vials. The label states it is for intravenous infusion only, sterile, with each vial containing 40 mg pantoprazole equivalent to 45.1 mg pantoprazole sodium. Distributed by Cardinal Health 107, LLC, originally from Wyeth Pharmaceuticals LLC, a Pfizer Inc. subsidiary, and made in France under license from Takeda GmbH. Storage instructions and warnings for institutional use are included.*
FDA Label Image

Chemical Structure (Protonix Iv 01)

Chemical Structure (Protonix Iv 01)
Chemical structure diagram of pantoprazole sodium, the active ingredient in Protonix I.V., showing its molecular framework with sodium and functional groups indicated.*
FDA Label Image

Protonix Iv 02

Protonix Iv 02
Packaging label for Protonix I.V. pantoprazole sodium injection powder for solution, 40 mg/10 mL, displaying distributor information. The label shows it is distributed by Vidal Pharmaceuticals LLC, a subsidiary of Pfizer Inc, based in Philadelphia, PA, and includes the Pfizer Injectables logo.*

* 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.