Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 83324-328

2 FDA label images from Chain Drug Marketing Association, Inc. · 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 Esomeprazole Magnesium (NDC 83324-328). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association, 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

Package Label-principal Display Panel (20 mg (14 Capsule Container Label))

Package Label-principal Display Panel (20 mg (14 Capsule Container Label))
Label for Esomeprazole Magnesium delayed-release capsules USP 20 mg by Chain Drug Marketing Association, Inc. The label states 14 capsules per package, one 14-day course of treatment, and highlights treatment for frequent heartburn. It includes directions, warnings, active ingredient information, and distributor details. The packaging is primarily yellow, white, and purple with Quality Choice branding.*
FDA Label Image

Package Label-principal Display Panel (20 mg (14 Capsule Container Carton))

Package Label-principal Display Panel (20 mg (14 Capsule Container Carton))
Packaging label for Esomeprazole Magnesium delayed-release capsules USP 20 mg by Chain Drug Marketing Association, Inc. The label states it treats frequent heartburn with a 14-capsule, 14-day course of treatment, taken once daily. The label includes drug facts with active ingredient, uses, warnings, directions, and manufacturer information. The package also features a barcode and references Quality Choice branding.*

* 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.