Diclofenac Sodium
Product Images NDC 67296-1480

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 67296-1480). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Label 25 100 Count (25mg Label)

Label of Diclofenac Sodium Delayed-Release Tablets, USP 25 mg, showing active ingredient strength and dosage form. The label includes directions to dispense Medication Guide, manufacturer details for BluePoint Laboratories, and a barcode. The label is marked Rx only and indicates a package size of 100 enteric-coated tablets.*

FDA Label Image

Label 50 Count 100 (50mg Label)

Label for Diclofenac Sodium Delayed-Release Tablets USP, 50 mg strength, containing 100 enteric-coated tablets. The label includes the labeler BluePoint Laboratories, barcode, NDC 68001-280-00, and storage instructions. It states Rx Only and advises pharmacists to dispense the enclosed medication guide.*

FDA Label Image

Label 75 Count 100 (75mg Label)

Packaging label for Diclofenac Sodium Delayed-Release Tablets, USP 75 mg. The label includes directions for pharmacists to dispense a Medication Guide with the product. It indicates 100 enteric-coated tablets per package. The label shows manufacturing details for BluePoint Laboratories, a barcode, storage instructions, and a caution to keep out of reach of children.*

FDA Label Image

Label 25 Count 100 (Image 01)

Label for Diclofenac Sodium Delayed-Release Tablets USP 25 mg, showing dosage strength and form. The label includes manufacturing details by Blue Point Laboratories, barcode, and storage instructions. It indicates 100 enteric-coated tablets and contains prescription-only labeling.*

FDA Label Image

Label 50 Count 100 (Image 02)

Label for Diclofenac Sodium Delayed-Release Tablets USP 50 mg, showing a package containing 100 enteric-coated tablets. The label indicates Rx only, with manufacturing information from Unique Pharmaceuticals & Biotec, India, and BluePoint Laboratories as the lab. It includes dosage instructions, storage conditions, and a barcode area for batch coding and 2D barcode printing.*

FDA Label Image

Label 25 Count 100 (Image 03)

Label for Diclofenac Sodium Delayed-Release Tablets USP, 75 mg strength. The label displays the NDC 68001-281-00 and indicates the product is Rx only. It includes directions for pharmacists to dispense a Medication Guide, and notes the package contains 100 enteric-coated tablets. Manufacturer details include BluePoint Laboratories and a Mumbai, India address. Storage instructions and a barcode are also visible.*

FDA Label Image

Structural Formula (Structural Formula)

Chemical structure of Diclofenac Sodium, showing a chlorinated aromatic ring connected via an amine group to a second aromatic ring bearing a sodium carboxylate substituent.*

* 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.