Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 68001-281

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 68001-281). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Diclofenac Sodium D-r Tablets, Usp 25mg 100 Ct (Rev 05-17)

Diclofenac Sodium D-r Tablets, Usp 25mg 100 Ct (Rev 05-17)
Label for Diclofenac Sodium Delayed-Release Tablets, USP 25 mg by BluePoint Laboratories. The label indicates 100 enteric-coated tablets with Rx only status. It includes manufacturer details, storage instructions, and a barcode for scanning. The package measures 118 mm by 31 mm and has a designated area for batch coding and 2D barcode.*
FDA Label Image

Diclofenac Sodium D-r Tablets, Usp 50mg 100 Ct (Rev 05-17)

Diclofenac Sodium D-r Tablets, Usp 50mg 100 Ct (Rev 05-17)
Label for Diclofenac Sodium 50 mg delayed-release tablets by BluePoint Laboratories. The label includes the drug name, strength, dosage form, NDC 68001-280-00, and a pharmacist instruction to dispense medication guide. It indicates a package of 100 enteric-coated tablets. A barcode and storage instructions are also visible.*
FDA Label Image

Diclofenac Sodium D-r Tablets, Usp 75mg 100 Ct (Rev 05-17)

Diclofenac Sodium D-r Tablets, Usp 75mg 100 Ct (Rev 05-17)
Label for Diclofenac Sodium Delayed-Release Tablets USP, 75 mg strength. The label states it contains 100 enteric-coated tablets and is manufactured for BluePoint Laboratories by Unique Pharma Chemical Laboratories in Mumbai, India. Includes NDC code 68001-281-00, directions for pharmacists to dispense the Medication Guide, storage instructions, and a barcode.*
FDA Label Image

Image 01

Image 01
Label for Diclofenac Sodium Delayed-Release Tablets, USP 25 mg by BluePoint Laboratories. The label indicates prescription use, with 100 enteric coated tablets per container. It includes the NDC 68001-279-00, barcode, manufacturing details, and storage instructions on a white background with blue and teal color accents.*
FDA Label Image

Image 02

Image 02
Label for Diclofenac Sodium 50 mg delayed-release tablets by BluePoint Laboratories. The label includes the NDC 68001-280-00 and specifies 100 enteric-coated tablets. It features dosage strength prominently, a pharmacist medication guide reminder, manufacturer details, and a barcode for scanning.*
FDA Label Image

Image 03

Image 03
Label from a box of Diclofenac Sodium Delayed-Release Tablets, USP 75 mg, oral dosage form. The label indicates it is manufactured for BluePoint Laboratories and contains 100 enteric-coated tablets. It includes the NDC 68001-281-00, pharmacist dispensing instructions, a barcode, and storage directions. The label also features the BluePoint Laboratories logo.*
FDA Label Image

Structural Formula (Structural Formula)

Structural Formula (Structural Formula)
Chemical structure of Diclofenac Sodium showing two aromatic rings, a chloride substitution, and a sodium acetic acid group attached.*

* 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.