Omeprazole Capsule, Delayed Release
Product Images NDC 0781-2234

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 0781-2234). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Structure (Image 01)

Chemical structure of omeprazole, showing the molecular arrangement with two aromatic rings, including methoxy groups and a sulfoxide functional group, consistent with the active ingredient in Omeprazole 40 mg delayed-release capsules by Sandoz Inc.*

FDA Label Image

40 mg Label (Image 02)

Omeprazole 40 mg delayed-release capsules, USP, prescription oral medication by Sandoz Inc. The label includes directions for use, storage instructions, a 30-capsule count, and an imprint area with spaces for date, lot number, and expiration. The label prominently shows the NDC number 0781-2234-31.*

* 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.