Etodolac Tablet, Film Coated, Extended Release
Product Images NDC 68382-272

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Etodolac (NDC 68382-272). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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

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Chemical structure diagram of Etodolac, showing its molecular arrangement including a benzene ring, nitrogen atom, and carboxylic acid group. The diagram illustrates the arrangement of atoms and bonds characteristic of Etodolac.*

FDA Label Image

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Label for Etodolac Extended-release Tablets, USP 400 mg film-coated tablets, oral dosage form, containing 100 tablets per container. The label includes storage instructions, dosage reference, and manufacturer information: Cadila Healthcare Ltd., India, distributed by Zydus Pharmaceuticals (USA) Inc. It also displays the NDC code 68382-271-01 and a note for pharmacists to dispense the medication guide separately.*

FDA Label Image

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Etodolac 500 mg Extended-release Tablets, USP film coated, extended release dosage form for oral use. The label shows a package of 100 tablets with Rx only designation. Manufactured by Cadila Healthcare Ltd., India, and distributed by Zydus Pharmaceuticals USA Inc. It includes storage instructions, dosage reference, and a medication guide notice for pharmacists.*

FDA Label Image

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Packaging label for Etodolac Extended-release Tablets, USP, 600 mg film-coated tablets by Zydus Pharmaceuticals USA Inc. The label states 100 tablets per container with Rx only. It includes storage instructions, dosage form, tablet strength, distributor information, and a barcode.*

* 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.