Protonix
Product Images NDC 21695-108

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Protonix (NDC 21695-108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Image Of Chemical Structure (Cfeacb5c 8b1b 48f6 9acf 00044a8179b4 01)

Chemical structure diagram of the active ingredient for Protonix, showing its molecular components including fluorine, sodium, sulfur, nitrogen atoms, and water of hydration (1.5 H2O).*

FDA Label Image

Protonix 40 mg (Cfeacb5c 8b1b 48f6 9acf 00044a8179b4 02)

Protonix 40 mg delayed-release tablets label for a 15-count package. Each tablet contains 40 mg of pantoprazole sodium. The label includes NDC 21695-108-15, manufacturer Wyeth Pharmaceuticals Inc., Philadelphia, PA, and states RX only. It also bears the Physician Partner logo and storage instructions.*

* 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.