Pantoprazole Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 72572-553

View Photos of 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 Pantoprazole Sodium (NDC 72572-553). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Structure (Pantoprazole Sodium For Injection Civica 1)

Structure (Pantoprazole Sodium For Injection Civica 1)
Chemical structure of Pantoprazole Sodium showing its molecular configuration with fluorine, oxygen, nitrogen, sodium ion, and associated methoxy groups as depicted in the diagram.*
FDA Label Image

Unit (Pantoprazole Sodium For Injection Civica 2)

Unit (Pantoprazole Sodium For Injection Civica 2)
Pantoprazole Sodium for Injection 40 mg vial label for intravenous infusion. The label includes dosage information, storage instructions (store at 20 to 25°C, do not freeze), and specifies a sterile single-dose vial. The product is manufactured by Civica, Inc., located in Lehi, Utah. The label highlights the drug's prescription-only status and cautions about proper usage and storage.*
FDA Label Image

Carton Label (Pantoprazole Sodium For Injection Civica 3)

Carton Label (Pantoprazole Sodium For Injection Civica 3)
The packaging label for Pantoprazole Sodium Injection, Powder, Lyophilized, for Solution, 40 mg per vial, by Civica, Inc. It is indicated for intravenous infusion only, supplied in a carton containing 10 vials with no filter required. The label includes instructions to protect from light and directions for use and storage.*

* 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.