Pantoprazole Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 65219-385

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 65219-385). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Description (Pan0a 0000 01)

Chemical structure of pantoprazole sodium showing the molecular arrangement with labels for sodium (Na+) and water of hydration (1.5 H2O).*

FDA Label Image

Logo Black-fk (Pan0a 0000 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Pantoprazole Sodium for Injection Vial Label)

Label for Pantoprazole Sodium for Injection 40 mg per vial, lyophilized powder for intravenous infusion. The label indicates it is a sterile, single-dose vial for intravenous use only, requiring reconstitution. It is manufactured by Fresenius Kabi USA, LLC and includes storage instructions between 20 to 25°C with protection from light. The label features a barcode and NDC 65219-385-01.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Pantoprazole Sodium for Injection Tray Label)

Pantoprazole Sodium for Injection 40 mg per vial, lyophilized powder for intravenous infusion supplied by Fresenius Kabi USA, LLC. The label indicates each vial contains 40 mg pantoprazole (equivalent to 45.1 mg pantoprazole sodium). The product is sterile, single-dose, and requires reconstitution before use. Storage recommendations and manufacturer contact information are also shown.*

* 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.