Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 67296-2215

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 67296-2215). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

25 mg 60 Count Bottle Label (Dcs 25 mg 60 Count)

Label for Diclofenac Sodium Delayed-Release Tablets USP 25 mg, showing a bottle or carton label with red and black text. It indicates 60 tablets, manufactured and distributed by Carlsbad Technology, Inc., Carlsbad, CA. The label includes storage instructions, a pharmacist dispensing note, and a barcode.*

FDA Label Image

Dcs 50 mg 60 Count (Dcs 50 mg 60 Count)

Label for Diclofenac Sodium Delayed-Release Tablets USP, 50 mg strength. The label states it is for prescription use only and includes handling instructions, storage conditions (20° to 25°C), and a warning to keep medication out of children's reach. It lists manufacture and distribution by Carlsbad Technology, Inc. The package contains 60 tablets.*

FDA Label Image

Dcs 75 mg 60 Count (Dcs 75 mg 60 Count)

Label for Diclofenac Sodium Delayed-Release Tablets USP, 75 mg, oral tablets. The label shows the product name, strength, and dosage form with a quantity of 60 tablets. It includes instructions for pharmacists to dispense with a medication guide and storage conditions, along with manufacturer information from Carlsbad Technology, Inc.*

FDA Label Image

Figure (Dic05 0006 01)

Chemical structure of Diclofenac Sodium, showing the arrangement of chlorine atoms, carboxylate group, and aromatic rings typical of this nonsteroidal anti-inflammatory drug.*

* 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.