Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 55154-2645

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 55154-2645). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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

Bag Label (6229247e Ee15 466e A8ac Adcd646b738d 00)

Bag Label (6229247e Ee15 466e A8ac Adcd646b738d 00)
Pantoprazole sodium delayed-release tablets, USP 40 mg help reduce acid levels in the stomach. Each tablet contains Pantoprazole sodium USP equivalent to pantoprazole 40 mg. They should not be split, chewed, or crushed. The usual dosage is indicated in the package insert along with prescribing information and warnings. Store at 68-77° F (20-25° C). This medication guide must be dispensed by pharmacists. This is an institutional use package and not intended for home use. Keep them out of the reach of children. Aurobindo Phamma USA, Inc. produces it. Major pharmaceuticals distribute it through Cardinal Health, in Dublin, OH. The text seems complete and useful.*
FDA Label Image

Chemical Structure (Pantoprazole Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.