Oxaprozin Tablet, Film Coated
Product Images NDC 55111-170

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Oxaprozin (NDC 55111-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories 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

Container

Label for Oxaprozin Tablets, USP 600 mg film-coated tablets. The label indicates 100 tablets per package, prescription use only, manufactured by Dr. Reddy's Laboratories Limited in India. Storage instructions and dispensing information are provided. The label includes an NDC number 55111-170-01 and barcode.*

FDA Label Image

Structure (Structure)

Chemical structure of Oxaprozin, showing its molecular arrangement including aromatic rings, an oxazole ring, and a carboxylic acid functional group.*

* 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.