Omeprazole
Product Images NDC 11383-257

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 11383-257). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Weeks & Leo Co., 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

14 Tablet Box Front (Omeprazole 1)

Omeprazole Delayed Release Tablets 20 mg packaging label from Weeks & Leo Co., Inc. The label indicates 14 tablets in the package, intended as a one 14-day course of treatment. It highlights the product as an acid reducer for frequent heartburn occurring 2 or more days a week. Additional text includes comparison to Prilosec OTC active ingredient and standard packaging elements like barcode, NDC number 11383-257-16, and tamper-evident warnings.*

FDA Label Image

14 Tablet Box Rear (Omeprazole 2)

Drug Facts panel for Omeprazole Delayed Release 20 mg tablets by Weeks & Leo Co., Inc. The panel details active ingredient, intended use for frequent heartburn, allergy alert, warnings, advice to consult a doctor, directions for 14-day use, and precautions for pregnant women, breastfeeding, and children under 18.*

FDA Label Image

Blister Label (Omeprazole 3)

Label of Omeprazole Delayed Release (DR) Tablets 20 mg by Weeks & Leo Co., Inc. The label includes instructions to push the tablet through foil and warnings not to chew or crush the tablets or crush them in food. Manufacturer information shows Dexcell Ltd., located at 1 Dexcell St., Or Akiva, Israel.*

* 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.