Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 51655-744

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 51655-744). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 744 52 Master Bottle Label Approval Rev A 07 21)

NDC 51655-744-52 is a medication with the active ingredient Pantoprazole Sodium in Delayed-Release Tablets, USP with a strength of 20mg, and comes in a container of 30 tablets that are not to be split, chewed or crushed before administration. The dosage should be checked on the package insert and it should be stored at a controlled room temperature between 20° to 25°C. The exact GTIN is not available. The medication should be kept out of the reach of children and stored in its original container. This product is a repackaged version of the original product with LCN# 00 and Rev. A.*

FDA Label Image

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Structure.jpg (Structure)

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