Omeprazole Capsule, Delayed Release
Product Images NDC 50090-6720

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 50090-6720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 Image (Lbl500906720)

Label Image (Lbl500906720)
Label for Omeprazole 40 mg delayed-release capsules by A-S Medication Solutions shows product and lot numbers, storage instructions to keep between 60 to 77 degrees Fahrenheit and protect from light and moisture, and package quantity of 30 capsules. The label includes a QR code and barcode with dosage instruction to see package insert.*
FDA Label Image

Pic1 (Pic1)

Pic1 (Pic1)
Omeprazole 20 mg capsule, delayed release. The image shows a clear capsule with green and white halves and the imprint 'OMEPRAZOLE 20 mg' on it. This product is manufactured by A-S Medication Solutions for oral administration.*
FDA Label Image

Pic2 (Pic2)

Pic2 (Pic2)
The image shows a label for Omeprazole 40 mg delayed-release capsules. The label displays the proprietary and generic name Omeprazole along with the strength of 40 mg. The style suggests it is part of the product packaging or an identification label for the capsules by A-S Medication Solutions.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Omeprazole showing its molecular arrangement including sulfoxide group and aromatic rings. The structure depicts the two ring systems and functional groups characteristic of Omeprazole's chemical composition.*

* 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.