Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 61442-102

7 FDA label images from Carlsbad Technology, Inc. · 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 61442-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carlsbad Technology, 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

Figure (Dic05 0006 01)

Figure (Dic05 0006 01)
Chemical structure of Diclofenac Sodium, the active ingredient, showing its molecular arrangement with chlorinated aromatic rings and a carboxylate group.*
FDA Label Image

Figure (Dic05 0006 02)

Figure (Dic05 0006 02)
Diclofenac Sodium Delayed Release 50 mg oral tablets by Carlsbad Technology, Inc. The carton displays the product name, dosage strength, delayed release tablet form, and quantity of 100 tablets (5 bottles of 100 each). The packaging is primarily white with blue and orange accents.*
FDA Label Image

Figure (Dic05 0006 03)

Figure (Dic05 0006 03)
The image shows a blister card containing ten 50 mg delayed release tablets of Diclofenac Sodium. The tablets are small, round, yellow, and marked with the number '101'. The blister pack is designed for oral administration and is labeled under Carlsbad Technology, Inc.*
FDA Label Image

Figure (Dic05 0006 04)

Figure (Dic05 0006 04)
Diclofenac Sodium Delayed Release 75 mg oral tablets in a clear blister pack, containing 10 tablets. The label on the blister shows the strength (75 mg) and the product name (Diclofenac Sodium Delayed Release). Manufactured by Carlsbad Technology, Inc.*
FDA Label Image

Principal Display Panel – Bottle Label (Dic05 0006 05)

Principal Display Panel – Bottle Label (Dic05 0006 05)
Label for Diclofenac Sodium Delayed-Release Tablets USP, 25 mg strength. The label states the product contains delayed-release tablets with each tablet containing 25 mg of Diclofenac Sodium USP. It is distributed by Carlsbad Technology, Inc. and the package contains 60 tablets. The label includes storage instructions and a pharmacist dispensing note, with a barcode and space for lot number and expiration date.*
FDA Label Image

Principal Display Panel – Bottle Label (Dic05 0006 06)

Principal Display Panel – Bottle Label (Dic05 0006 06)
Label for Diclofenac Sodium Delayed-Release Tablets USP, 50 mg strength. The label includes dosage form (tablets), quantity (60 tablets), labeler Carlsbad Technology, Inc., and handling instructions. It features a barcode and notes the product is prescription only with storage and dispensing guidelines.*
FDA Label Image

Principal Display Panel – Bottle Label (Dic05 0006 07)

Principal Display Panel – Bottle Label (Dic05 0006 07)
Label for Diclofenac Sodium Delayed-Release Tablets USP 75 mg by Carlsbad Technology, Inc. The label includes medication strength (75 mg), quantity (60 tablets), and instructions for dispensing and storage temperatures. The NDC number 61442-103-60 and barcode are visible, along with a warning to dispense with the medication guide.*

* 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.