Etodolac
Product Images NDC 70332-320

3 FDA label images from California Pharmaceuticals, Llc · 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 70332-320). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by California Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Cs174-a1 Repackaged Etodolac (Cs174 A1 Repackaged Etodolac)

Cs174-a1 Repackaged Etodolac (Cs174 A1 Repackaged Etodolac)
Etodolac Extended-Release 600 mg Tablets, USP label shows the product name and strength. The package contains 7 tablets. The label indicates the manufacturer as Cadila Healthcare Ltd., Ahmedabad, India, with repackaging and distribution by California Pharmaceuticals, LLC, Camarillo, CA. Storage instructions and a barcode are also visible.*
FDA Label Image

Cs174-a2 Repackaged Etodolac (Cs174 A2 Repackaged Etodolac)

Cs174-a2 Repackaged Etodolac (Cs174 A2 Repackaged Etodolac)
Label for Etodolac Extended Release 600 mg Tablets, USP, containing 30 tablets. Each tablet has 600 mg of Etodolac. The label is marked Rx Only and indicates manufacturing by Cadila Healthcare Ltd., India. It is repackaged and distributed by California Pharmaceuticals, LLC, Camarillo, CA. The label includes storage instructions and a barcode with NDC 70332-320-02.*
FDA Label Image

Etodolac-01 (Etodolac 01)

Etodolac-01 (Etodolac 01)
Chemical structure of Etodolac showing its molecular composition and arrangement with a characteristic fused ring system, including a benzene ring and a carboxylic acid group attached to the bicyclic framework.*

* 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.