Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 63868-425

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 63868-425). 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

Carton (Carton)

The packaging label for Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg, containing 14 capsules for a one 14-day course of treatment. The label highlights its use for treating frequent heartburn occurring 2 or more days a week. It includes drug facts, directions, warnings, inactive ingredients, and tips for managing heartburn. The labeler is Chain Drug Marketing Association Inc, with NDC 63868-425-14, and states the product is made in India.*

FDA Label Image

Container

Drug Facts label for Esomeprazole Magnesium 20 mg delayed-release capsules includes active ingredient, purpose, uses, warnings, allergy information, directions, and inactive ingredients. It details treatment for frequent heartburn up to 14 days and emphasizes not using the product beyond this period without medical advice. The label instructs users to swallow capsules whole and lists precautions for children and certain medical conditions.*

* 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.