Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 72189-112

2 FDA label images from Direct Rx · 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 72189-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

30 (72189 112 30)

30 (72189 112 30)
Label for PANTOPRAZOLE SODIUM delayed-release tablets, 20 mg strength, with a package count of 30 tablets. The label indicates the generic version for Protonix and states the active ingredient as pantoprazole sodium sesquihydrate equivalent to 20 mg pantoprazole. The product is packaged and distributed by DirectRx, and the label includes lot number 12JN2007 and expiration date 12/31/21.*
FDA Label Image

60 (72189 112 60)

60 (72189 112 60)
Label for PANTOPRAZOLE SODIUM delayed-release tablets, 20 mg strength, containing 60 tablets per container. The label notes it as a generic for Protonix and states the drug is pantoprazole sodium sesquihydrate USP equivalent to pantoprazole 20 mg. Distributed by DIRECT RX, with lot and expiration details visible.*

* 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.