Omeprazole Capsule, Delayed Release
Product Images NDC 70700-151

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 70700-151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xiromed, 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

Ome-10mg-30count (Ome 10mg 30count)

Label for Omeprazole Delayed-Release Capsules, USP, 10 mg strength, oral capsule dosage form. The package contains 30 capsules, labeled for prescription use by Xiromed, LLC. Storage instructions and handling precautions are provided. The label displays the NDC 70700-149-30 and notes the product is made in Spain.*

FDA Label Image

Ome-20mg-100count (Ome 20mg 100count)

Omeprazole 20 mg delayed-release capsules, USP, oral dosage form, 100 capsules per container, manufactured by Xiromed, LLC. The label includes storage instructions, dispensing requirements, and a QR code for a medication guide. It is marked Rx only and produced in Spain.*

FDA Label Image

Ome-20mg-100count (Omep 40mg)

Label for Omeprazole Delayed-Release Capsules USP 40 mg by Xiromed, LLC. The label highlights prescription status, storage instructions, and the package contains 1000 capsules. It notes that each capsule contains 40 mg of Omeprazole and includes handling and safety instructions. The product is manufactured in Spain.*

FDA Label Image

Structure (Image 01)

Chemical structure of Omeprazole, showing the molecular arrangement including a benzimidazole ring system with a methoxy group, a sulfoxide functional group, and a pyridine ring with methyl and methoxy substituents.*

* 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.