Omeprazole Capsule, Delayed Release
Product Images NDC 60687-608

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 60687-608). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp60801

Omeprazole 40 mg delayed-release capsule for oral use. The capsule is two-toned with a light beige upper half displaying the imprint 'OMEPRAZOLE 40 mg' and a purple lower half with the imprint 'R645'. Manufactured by American Health Packaging.*

FDA Label Image

40 mg Omeprazole Delayed-release Capsule Blister (Blister)

Multiple identical labels for Omeprazole delayed-release capsules, USP 40 mg, manufactured by American Health Packaging. Each label shows the product name, strength, dosage form, barcode, and space placeholders for expiration date and lot number.*

FDA Label Image

40 mg Omeprazole Delayed-release Capsules Carton (Carton)

Label for Omeprazole delayed-release capsules, USP, 40 mg strength in a 100-capsule package (10 x 10). The label includes the National Drug Code (NDC) 60687-608-01, with directions for pharmacists to dispense the accompanying medication guide, and storage instructions to protect from light and moisture. Distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

Structural Formula (Structure)

Chemical structure diagram of Omeprazole, illustrating the molecular arrangement of atoms in the active ingredient. The image shows functional groups and bonds typical of Omeprazole's structure used in its pharmaceutical formulation as a delayed-release oral capsule by American Health Packaging.*

* 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.