Pantoprazole Sodium Injection, Powder, For Solution
Product Images NDC 71288-600

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 71288-600). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Carton (Panto Vz Carton)

Packaging label for Pantoprazole Sodium Injection, 40 mg per vial, powder for solution for intravenous infusion. The label states it is preservative-free, sterile, and for single-dose vials, packaged in quantities of 10. The labeler is Meitheal Pharmaceuticals Inc., with a barcode and NDC 71288-600-92. Storage instructions and manufacturing details are also present.*

FDA Label Image

Structural Formula (Panto Vz Structure)

Chemical structure diagram of pantoprazole sodium, depicting its molecular framework including methoxy, difluoromethoxy groups, and the sodium ion.*

FDA Label Image

Principal Display Panel – Pantoprazole Sodium For Injection, 40 mg Vial Label (Panto Vz Vial)

Label for Pantoprazole Sodium for Injection 40 mg per vial, intended for intravenous infusion only. The label states it is a sterile, single-dose vial and instructs to discard unused portions. Manufactured by Meitheal Pharmaceuticals Inc., Chicago, IL, made in China. Includes NDC 71288-600-91 and dosage instructions for reconstitution and administration.*

* 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.