Omeprazole 20 Mg Tablet, Delayed Release
Product Images NDC 25000-094

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omeprazole 20 Mg (NDC 25000-094). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marksans Pharma Limited, 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

Omeprazole-wbm-14s-blister-carton- (Omeprazole Wbm 14s Blister Carton)

Omeprazole-wbm-14s-blister-carton- (Omeprazole Wbm 14s Blister Carton)
Omeprazole 20 mg delayed-release tablets box from Marksans Pharma Limited. The label states the product is an acid reducer for treating frequent heartburn with 14 tablets in the package. The box highlights a 14-day treatment course and includes dosing and drug facts information. The label notes the wildberry mint coated tablet shape with instructions to swallow without chewing.*
FDA Label Image

Omeprazole-wbm-14s-bottle-carton- (Omeprazole Wbm 14s Bottle Carton)

Omeprazole-wbm-14s-bottle-carton- (Omeprazole Wbm 14s Bottle Carton)
Packaging label for Omeprazole 20 mg delayed-release tablets by Marksans Pharma Limited. The label shows a 14-tablet carton labeled as an acid reducer for treating frequent heartburn. The tablet is described as a wildberry mint coated tablet, to be swallowed whole and not chewed. The label includes detailed Drug Facts, active ingredient information, directions, warnings, inactive ingredients, and customer contact information. The NDC is 25000-094-76.*
FDA Label Image

Omeprazole-wbm-14s-bottle-label (Omeprazole Wbm 14s Bottle Label)

Omeprazole-wbm-14s-bottle-label (Omeprazole Wbm 14s Bottle Label)
Drug Facts panel for Omeprazole 20 mg delayed-release tablets by Marksans Pharma Limited. The text includes active ingredient details, purpose as an acid reducer, usage instructions, warnings such as allergy alert and when to ask a doctor, directions for 14-day treatment, and storage information. The panel also features a tamper-evident warning and contact information for questions.*

* 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.