Fondaparinux Sodium Powder
NDC Package 62227-006-03

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Fondaparinux Sodium powders is fondaparinux is used to treat serious blood clots in the legs and/or lungs. This formulation utilizes a powder delivery system. Marketed by Brightgene Bio-medical Technology Co., Ltd., this product is identified by NDC 62227-006.

Identification & Billing

NDC Package Code
62227-006-03
Package Description
400 g in 1 BAG
Product Code
62227-006
11-Digit Billing Format
62227000603

Clinical Specifications

Proprietary Name
Fondaparinux Sodium
Non-Proprietary Name
Fondaparinux Sodium
Substance Name
Fondaparinux Sodium
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s)
FONDAPARINUX SODIUM 1 g/g
Usage Information
Fondaparinux is used to treat serious blood clots in the legs and/or lungs. It is usually used with another "blood thinner" medication (warfarin). If untreated, blood clots can travel to the lungs, heart, or brain, causing serious (possibly fatal) breathing problems, heart attack, or stroke. This drug may also be used to prevent blood clots after certain surgeries with an increased risk of blood clots (such as hip fracture, abdominal, knee/hip replacement). Fondaparinux is known as a "blood thinner" (anticoagulant). It is a drug similar to heparin that works by blocking certain natural substances in the blood that cause clotting.

Regulatory & Marketing

Labeler Name
Brightgene Bio-medical Technology Co., Ltd.
Product Type
Bulk Ingredient
Marketing Category
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date
02-01-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 62227-006-03 identifies a specific commercial package of 400 g in 1 bag of Fondaparinux Sodium (UNFINISHED drug), a bulk ingredient labeled by Brightgene Bio-medical Technology Co., Ltd.. This powder is formulated for use and contains fondaparinux sodium as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Brightgene Bio-medical Technology Co., Ltd. on February 01, 2019. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Fondaparinux is used to treat serious blood clots in the legs and/or lungs. It is usually used with another "blood thinner" medication (warfarin). If untreated, blood clots can travel to the lungs, heart, or brain, causing serious (possibly fatal) breathing problems, heart attack, or stroke. This drug may also be used to prevent blood clots after certain surgeries with an increased risk of blood clots (such as hip fracture, abdominal, knee/hip replacement). Fondaparinux is known as a "blood thinner" (anticoagulant). It is a drug similar to heparin that works by blocking certain natural substances in the blood that cause clotting.

How is this Brightgene Bio-medical Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62227000603. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
62227-006-03
11-Digit CMS (5-4-2)
62227-0006-03

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.