Etodolac Tablet, Film Coated
Product Images NDC 51655-735

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Etodolac (NDC 51655-735). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 735 52 Master Bottle Label Approval Rev A 06 21)

Label (51655 735 52 Master Bottle Label Approval   Rev A 06 21)
Label for Etodolac Tablets, USP 500 mg, film-coated oral tablets. The package contains 30 tablets and is labeled for prescription use only (Rx Only). Storage instructions specify temperatures between 20°-25°C (68°-77°F). Labeler is Northwind Health Company, LLC.*
FDA Label Image

Formula (Etodolac Tablets Usp 1)

Formula (Etodolac Tablets Usp 1)
Chemical structure of Etodolac showing its molecular framework with ethyl groups, a nitrogen atom, an oxygen atom in a ring, and a carboxylic acid 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.