Esomeprazole Magnesium Tablet, Delayed Release
Product Images NDC 0363-0361

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 0363-0361). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Co., 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 Tablets))

Drug facts label for Esomeprazole Magnesium delayed-release tablets, 20 mg strength, marketed by Walgreens Co. The label provides directions, warnings, active ingredient information, and usage instructions for a 14-day course of treatment to reduce acid and treat frequent heartburn. It includes allergy alerts, overdose advice, and storage conditions, emphasizing a once-daily oral dose.*

FDA Label Image

Package Label-principal Display Panel (20 mg (14 Tablets))

Esomeprazole Magnesium 20 mg delayed-release tablets packaging label by Walgreens Co. The label indicates the product contains 42 tablets, divided into 3 bottles of 14 each, for treating frequent heartburn. It features warnings, directions, inactive ingredients, tips for managing heartburn, and a barcode. Manufactured in India, the product is an oral acid reducer with a 24-hour effect.*

* 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.