Omeprazole Capsule, Delayed Release
Product Images NDC 83324-309

2 FDA label images from Chain Drug Marketing Association, Inc. · 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 Omeprazole (NDC 83324-309). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association, 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

Package Label-principal Display Panel (20 mg (14 Capsules Bottle))

Package Label-principal Display Panel (20 mg (14 Capsules Bottle))
Label for Omeprazole 20 mg delayed-release capsules, oral use, from Chain Drug Marketing Association, Inc. The label includes the product name, strength, dosage form, quantity of 14 capsules, and usage information such as treating frequent heartburn with a 14-day course. It features a Quality Choice seal, warnings, directions for use, and manufacturer contact details. The label design includes multiple panels with text in black, purple, green, and blue on a white background.*
FDA Label Image

Package Label-principal Display Panel (20 mg Container Carton Label)

Package Label-principal Display Panel (20 mg Container Carton Label)
Omeprazole Delayed-Release Capsules USP 20 mg packaging label from Chain Drug Marketing Association, Inc. The carton features a blue and purple design with product and usage information, indicating 14 capsules for a 14-day treatment course. It highlights the product's purpose as an acid reducer for frequent heartburn and includes usage, warnings, and drug facts sections surrounding the main panel.*

* 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.