Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 46122-736

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 46122-736). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amerisource Bergen, 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))
Packaging label for Esomeprazole Magnesium delayed-release capsules USP 20 mg by AmerisourceBergen. The label includes product details such as the indication for frequent heartburn treatment and instructions noting a 14 capsules count per package for a 1 to 4-day treatment course. The label also highlights warnings, directions, ingredient information, and manufacturer details.*
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))
Esomeprazole Magnesium 20 mg delayed-release capsules packaging label by Amerisource Bergen. The package contains 14 capsules for one 14-day course of treatment. The front panel highlights acid reducer use for frequent heartburn and includes a product image. Drug Facts panels on the sides provide active ingredient details, usage instructions, warnings, directions, inactive ingredients, and consumer information. The bottom panel includes barcode and lot/expiry placeholders.*

* 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.