Protonix Injection, Powder, For Solution
Product Images NDC 0008-0923

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Protonix (NDC 0008-0923). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer 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

Chemical Structure (Protonix Iv 01)

Chemical structure of pantoprazole sodium, the active ingredient in Protonix I.V. injection powder for solution, showing its molecular composition and arrangement.*

FDA Label Image

Principal Display Panel (40 mg Vial Label)

FDA Label Image

Principal Display Panel (40 mg Vial Carton)

Label for Protonix I.V. (pantoprazole sodium) injection powder for solution, 40 mg per vial. The sterile, single-dose vial is intended for intravenous infusion. The label includes storage instructions, manufacturer information listed as Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc., and indicates reconstitution is required before use.*

FDA Label Image

Principal Display Panel (25 Vial Carton)

Packaging label for Protonix I.V. (pantoprazole sodium) 40 mg/vial injection powder for solution. The label indicates a sterile, single-dose vial for intravenous infusion only, containing 1 mg edetate disodium. Labeler is Wyeth Pharmaceuticals LLC, a Pfizer subsidiary. Storage instructions and distribution information are included. The label includes barcodes and a space for lot and expiration dates.*

FDA Label Image

Principal Display Panel (10 Vial Carton Package Label)

Packaging label for Protonix I.V. (pantoprazole sodium) Injection, powder for solution, 40 mg per vial. The carton contains 25 vials and is labeled for intravenous infusion only. The product is distributed by Wyeth Pharmaceuticals LLC, a Pfizer subsidiary. Storage instructions and ingredient details are also visible on the label. The NDC number is 0008-0923.*

FDA Label Image

Protonix Iv 06

Label for Protonix I.V. (pantoprazole sodium) injection powder for solution, 40 mg per vial, sterile for intravenous infusion. The label notes a single-dose vial, distributed by Wyeth Pharmaceuticals LLC, a Pfizer subsidiary. Storage instructions and formulation details are also included alongside barcodes and lot/expiration placeholders.*

* 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.