Etodolac Tablet, Film Coated, Extended Release
Product Images NDC 0093-7172

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Etodolac (NDC 0093-7172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva 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.

Product Images & Figures Index

FDA Label Image

Image 1

Image 1
Chemical structure of Etodolac, illustrating its molecular composition and arrangement of atoms typical for this nonsteroidal anti-inflammatory drug.*
FDA Label Image

Image 2

Image 2
Etodolac Extended-Release Tablets, USP 400 mg, film-coated oral tablets in a pack of 100. The label shows the labeler as Teva Pharmaceuticals USA, Inc. The label includes a NDC number 00093-1122-01 and instructions for the pharmacist to dispense the accompanying Medication Guide to each patient.*
FDA Label Image

Image 3

Image 3
Etodolac Extended-Release Tablets, USP 500 mg film-coated tablets in a bottle label format. The label shows the strength, dosage form as oral extended-release tablets, NDC 0093-7172-01, and is labeled for pharmacist use with instructions to dispense the accompanying medication guide. The bottle contains 100 tablets and is manufactured by Teva Pharmaceuticals USA, Inc.*
FDA Label Image

Image 4

Image 4
Label for Etodolac Extended-Release Tablets, USP 600 mg by Teva Pharmaceuticals USA, Inc. It displays the 600 mg strength, dosage form as film coated extended-release tablets, oral route, NDC 0033-1118-01, and packaging quantity of 100 tablets. The label includes medication guide dispensing instructions and serialization coding area.*

* 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.