Omeprazole Tablet, Delayed Release
Product Images NDC 43598-841

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 43598-841). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddys Laboratories 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

Carton (Carton)

Packaging label for Omeprazole Delayed-Release Tablets 20 mg by Dr. Reddys Laboratories Inc. The label highlights its use as an acid reducer for frequent heartburn relief. The box contains 42 tablets, providing three 14-day courses of treatment. The label features a purple color scheme and includes a barcode, safety seal warning, and bottle image with dosage and product details.*

FDA Label Image

Container (Container)

Omeprazole 20 mg delayed-release tablets by Dr. Reddys Laboratories Inc. The label states it is an acid reducer with 14 tablets per package, intended for oral use. The packaging highlights treatment for frequent heartburn and includes safety and usage information, warnings, directions, and inactive ingredients. The NDC is 43598-841.*

* 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.