Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 70518-0627

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 70518-0627). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Diclofenac Sodium 75mg 70518 0627 00

Label for Diclofenac Sodium Delayed-Release 75 mg tablets, quantity of 30. The label shows the product as a prescription drug repackaged by RemedyRepack Inc. It includes NDC number, manufacturer information, and storage directions. The label emphasizes delayed-release oral tablets manufactured by Carlsbad Tech, Inc.*

FDA Label Image

Mm2 (Diclofenac Sodium 75mg 70518 0627 01)

Label for Diclofenac Sodium Delayed-Release 75 mg oral tablets by RemedyRepack Inc. The label includes the drug name, strength, dosage form, quantity of 90 tablets, and FDA-required details such as NDC number 70518-0627, manufacturer information, storage conditions, and a QR code.*

FDA Label Image

Diclofenac Sodium 75mg 70518 0627 02

Label for Diclofenac Sodium Delayed-Release 75 mg oral tablets. The label indicates a quantity of 60 tablets and includes the NDC number 70518-0627-02. It is manufactured by Carlsbad Tech, Inc., Carlsbad, CA, and repackaged by RemedyRepack Inc. The label contains storage instructions and a barcode along with a 2D matrix code.*

FDA Label Image

Figure (Dic05 0006 01)

Chemical structure of Diclofenac Sodium, showing two chlorinated aromatic rings and a carboxylate group linked to the molecule, consistent with the active ingredient in Diclofenac Sodium Delayed Release tablets.*

* 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.