Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 70000-0731

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 Esomeprazole Magnesium (NDC 70000-0731). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leader/ Cardinal Health 110, 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.

Product Images & Figures Index

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 20 mg delayed-release capsules by LEADER/ CARDINAL HEALTH 110, INC. The label states 24 Hour Capsules, 14 capsules per package, designed for a one 14-day course of treatment to treat frequent heartburn. Includes warnings, active ingredient details, usage instructions, and manufacturer information. The label shows NDC 70000-0731-2 and notes it is made in India.*
FDA Label Image

Package Label-principal Display Panel (20 mg (28 Capsule Container Carton))

Package Label-principal Display Panel (20 mg (28 Capsule Container Carton))
Packaging label for ESOMEPRAZOLE MAGNESIUM delayed-release capsules USP, 20 mg by LEADER/ CARDINAL HEALTH 110, INC. The label highlights 24-hour acid reducer capsules, with 28 capsules (2 bottles of 14) per package, equivalent to two 14-day treatment courses. It includes Drug Facts, directions, warnings, and a comparison to a branded product. The label features a red and white design with the LEADER logo and barcode.*

* 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.