Esomeprazole Magnesium Delayed-release 20 Mg Mini Capsule, Delayed Release
Product Images NDC 25000-112

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 Delayed-release 20 Mg Mini (NDC 25000-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marksans Pharma Limited, 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

Esomeprazole-dr-20mg-14s-bottle-label (Esomeprazole Dr 20mg 14s Bottle Label)

Esomeprazole-dr-20mg-14s-bottle-label (Esomeprazole Dr 20mg 14s Bottle Label)
Label for Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg by Marksans Pharma Limited. The label indicates the product is an acid reducer used to treat frequent heartburn and contains 14 capsules intended for a 14-day course of treatment. Directions, warnings, active ingredient information, and manufacturer details are partially visible on the label.*
FDA Label Image

Esomeprazole-dr-20mg-14s-ifc-label (Esomeprazole Dr 20mg 14s Ifc Label)

Esomeprazole-dr-20mg-14s-ifc-label (Esomeprazole Dr 20mg 14s Ifc Label)
Packaging label for Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg by Marksans Pharma Limited. The label indicates 14 capsules per package for a 14-day course of treatment for frequent heartburn. The capsule image is shown with a purple and yellow color scheme. The label includes Drug Facts, directions, warnings, inactive ingredients, and contact information.*

* 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.