Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 49483-718

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 49483-718). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Time Cap Laboratories, 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

718t-esomeprazole-14ct-label (718t Esomeprazole 14ct Label)

718t-esomeprazole-14ct-label (718t Esomeprazole 14ct Label)
Esomeprazole Magnesium 20 mg delayed-release capsules carton label from Timely (TIME CAP LABORATORIES, INC.). It indicates 14 capsules for a 14-day course of treatment, marketed as an acid reducer for frequent heartburn, with directions and warnings listed on the side panel.*
FDA Label Image

718t-esomeprazole-42ct-carton (718t Esomeprazole 42ct Carton)

718t-esomeprazole-42ct-carton (718t Esomeprazole 42ct Carton)
Esomeprazole Magnesium 20 mg delayed-release capsules packaging label by Time Cap Laboratories, Inc. The label includes the product name, strength, and dosage form, highlights it as an acid reducer for frequent heartburn, and states it may take 1 to 4 days for full effect. The package contains 42 capsules, representing three 14-day treatment courses, with a comparison to Nexium 24HR. Additional drug facts, warnings, directions, inactive ingredients, and storage information appear on side panels. The label features a purple and orange gradient design with a purple-capped bottle image.*

* 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.