Omeprazole Tablet, Delayed Release
Product Images NDC 59726-744

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 59726-744). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by P & L Development, Llc, 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 Delayed-release Tablet 20 mg (equivalent To 20.6 mg Omeprazole Magnesium) (Omeprazole Magnesium Delayed Release Wildberry Tab 1)

Omeprazole Delayed-release Tablet 20 mg (equivalent To 20.6 mg Omeprazole Magnesium) (Omeprazole Magnesium Delayed Release Wildberry Tab 1)
This is a medication label containing information about drug facts, active ingredients, warnings, directions for use, and purpose. It includes details about a 24-hour delayed-release omeprazole tablets, comparison to Prilosec OTC, warnings against product misuse, and the manufacturer's contact information. Additionally, information is provided about a product called "Wellness Basics" for managing symptoms like night sweats and withdrawals, along with a wildberry flavor. It also highlights the purpose, active ingredients, and directions for use of a product called "Onegrane." The text ends with instructions on how to handle and contact in case of emergencies related to the product.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.