Etodolac Tablet, Film Coated
Product Images NDC 76385-119

3 FDA label images from Unichem Pharmaceuticals (usa), Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Etodolac (NDC 76385-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unichem Pharmaceuticals (usa), 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

Chemical Structure (Etodolac 01)

Chemical Structure (Etodolac 01)
Chemical structure of Etodolac, depicting the molecular arrangement including rings, carboxylic acid group, and substituents consistent with Etodolac's known chemical formula.*
FDA Label Image

Principal Display Panel 400 mg Container Label (Etodolac 04)

Principal Display Panel 400 mg Container Label (Etodolac 04)
Label for Etodolac Tablets USP, 400 mg strength, film-coated oral tablets. The package contains 100 tablets. Distributed by Bayshore Pharmaceuticals LLC, Short Hills, NJ, and manufactured by Aizant Drug Research Solutions Private Limited, Hyderabad, India. Includes storage instructions and a barcode.*
FDA Label Image

Principal Display Panel 500 mg Container Label (Etodolac 05)

Principal Display Panel 500 mg Container Label (Etodolac 05)
Label for Etodolac 500 mg film-coated tablets, USP, with a count of 100 tablets. The label includes NDC 76385-119-01, manufacturer details (Aizant Drug Research Solutions Private Limited, India), distributor info (Bayshore Pharmaceuticals LLC, NJ), and storage instructions at 20°C to 25°C. It also has a barcode and indicates the product is prescription only.*

* 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.