Pantoprazole Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 62756-129

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 62756-129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-pantoprazole-for-injection-chemical-structure (Spl Pantoprazole For Injection Chemical Structure)

Chemical structure of pantoprazole sodium, depicted with its molecular components including fluorinated aromatic rings, sulfur and nitrogen atoms, methoxy groups, sodium ion, and water of hydration.*

FDA Label Image

Spl-pantoprazole-for-injection-label (Spl Pantoprazole For Injection Label)

Pantoprazole Sodium for Injection 40 mg/vial lyophilized powder label for intravenous use. The label indicates each vial contains 40 mg of pantoprazole, requires reconstitution, and is for single-dose use. Distributed and manufactured by Sun Pharmaceutical Industries with storage instructions and lot/expiration fields.*

FDA Label Image

Spl-pantoprazole-for-injection-showbox (Spl Pantoprazole For Injection Showbox)

Packaging label for Pantoprazole Sodium injection powder, lyophilized, for solution. The label shows 40 mg per vial strength, intended for intravenous infusion only. It contains 1 mg edetate disodium, requires no filter, and includes one single-dose vial. Labeler is Sun Pharmaceutical Industries, Inc., with manufacturing in Gujarat, India.*

* 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.