Omeprazole Tablet, Delayed Release
Product Images NDC 59726-744

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)

This packaging label is for Omeprazole delayed-release tablets, 20 mg, by P & L Development, LLC. It includes 42 tablets designed for three 14-day courses of treatment. The label highlights the product as an acid reducer for frequent heartburn and shows tablets coated with wildberry flavor. The packaging also provides drug facts, warnings, directions, inactive ingredients, and contact information for questions or comments.*

* 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.