NDC Package 80425-0550-7 Diclofenac Sodium

Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
80425-0550-7
Package Description:
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Diclofenac Sodium
Non-Proprietary Name:
Diclofenac Sodium
Substance Name:
Diclofenac Sodium
Usage Information:
Diclofenac is used to relieve pain, swelling (inflammation), and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
11-Digit NDC Billing Format:
80425055007
Product Type:
Human Prescription Drug
Labeler Name:
Advanced Rx Of Tennessee, Llc
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA207714
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-27-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
80425-0550-11 BOTTLE in 1 CARTON / 112 g in 1 BOTTLE
80425-0550-115 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-5120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-640 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
80425-0550-8240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 80425-0550-7?

The NDC Packaged Code 80425-0550-7 is assigned to a package of 180 tablet, film coated in 1 bottle, plastic of Diclofenac Sodium, a human prescription drug labeled by Advanced Rx Of Tennessee, Llc. The product's dosage form is solution and is administered via topical form.

Is NDC 80425-0550 included in the NDC Directory?

Yes, Diclofenac Sodium with product code 80425-0550 is active and included in the NDC Directory. The product was first marketed by Advanced Rx Of Tennessee, Llc on August 27, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 80425-0550-7?

The 11-digit format is 80425055007. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-180425-0550-75-4-280425-0550-07