Omeprazole Capsule, Delayed Release
Product Images NDC 51655-061

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 51655-061). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 061 52 Master Bottle Label Approval Rev A 06 20)

Label for Omeprazole Delayed-Release Capsules USP 20 mg, containing 30 capsules. The label includes storage instructions for temperature and moisture control, mentions that the capsules should be swallowed whole, and provides manufacturer information for Northwind Health Company, LLC. It is a prescription-only oral capsule product.*

FDA Label Image

Structure (Structure)

Chemical structure diagram showing the molecular structure of omeprazole, the active ingredient in the medication. The structure includes the two main aromatic rings, sulfur, nitrogen, and oxygen atoms arranged in a configuration characteristic of omeprazole molecules.*

* 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.