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  5. NDC Package Code: 54868-5652-0 Arixtra

NDC Package 54868-5652-0 Arixtra

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
54868-5652-0
Package Description:
10 SYRINGE in 1 CARTON / .4 mL in 1 SYRINGE
Product Code:
54868-5652
Proprietary Name:
Arixtra
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.
11-Digit NDC Billing Format:
54868565200
NDC to RxNorm Crosswalk:
  • RxCUI: 861363 - fondaparinux sodium 5 MG in 0.4 ML Prefilled Syringe
  • RxCUI: 861363 - 0.4 ML fondaparinux sodium 12.5 MG/ML Prefilled Syringe
  • RxCUI: 861363 - fondaparinux sodium 5 MG per 0.4 ML Prefilled Syringe
  • RxCUI: 861364 - Atrixtra 5 MG in 0.4 ML Prefilled Syringe
  • RxCUI: 861364 - 0.4 ML fondaparinux sodium 12.5 MG/ML Prefilled Syringe [Arixtra]
Labeler Name:
Physicians Total Care, Inc.
Sample Package:
No
FDA Application Number:
NDA021345
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
12-07-2001
End Marketing Date:
06-30-2011
Listing Expiration Date:
06-30-2011
Exclude Flag:
D
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.

Frequently Asked Questions

What is NDC 54868-5652-0?

The NDC Packaged Code 54868-5652-0 is assigned to a package of 10 syringe in 1 carton / .4 ml in 1 syringe of Arixtra, labeled by Physicians Total Care, Inc.. The product's dosage form is and is administered via form.

Is NDC 54868-5652 included in the NDC Directory?

No, Arixtra with product code 54868-5652 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Physicians Total Care, Inc. on December 07, 2001 and its listing in the NDC Directory is set to expire on June 30, 2011 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 54868-5652-0?

The 11-digit format is 54868565200. 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
5-4-154868-5652-05-4-254868-5652-00