NDC Package 55150-232-02 Fondaparinux Sodium

Injection, Solution Subcutaneous - 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:
55150-232-02
Package Description:
2 SYRINGE, GLASS in 1 CARTON / .6 mL in 1 SYRINGE, GLASS (55150-232-00)
Product Code:
Proprietary Name:
Fondaparinux Sodium
Non-Proprietary Name:
Fondaparinux Sodium
Substance Name:
Fondaparinux Sodium
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:
55150023202
NDC to RxNorm Crosswalk:
  • RxCUI: 861356 - fondaparinux sodium 10 MG in 0.8 ML Prefilled Syringe
  • RxCUI: 861356 - 0.8 ML fondaparinux sodium 12.5 MG/ML Prefilled Syringe
  • RxCUI: 861356 - fondaparinux sodium 10 MG per 0.8 ML Prefilled Syringe
  • RxCUI: 861360 - fondaparinux sodium 2.5 MG in 0.5 ML Prefilled Syringe
  • RxCUI: 861360 - 0.5 ML fondaparinux sodium 5 MG/ML Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Eugia Us Llc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA206918
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-26-2017
    Listing Expiration Date:
    12-31-2025
    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
    55150-232-1010 SYRINGE, GLASS in 1 CARTON / .6 mL in 1 SYRINGE, GLASS (55150-232-00)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55150-232-02?

    The NDC Packaged Code 55150-232-02 is assigned to a package of 2 syringe, glass in 1 carton / .6 ml in 1 syringe, glass (55150-232-00) of Fondaparinux Sodium, a human prescription drug labeled by Eugia Us Llc. The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 55150-232 included in the NDC Directory?

    Yes, Fondaparinux Sodium with product code 55150-232 is active and included in the NDC Directory. The product was first marketed by Eugia Us Llc on December 26, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55150-232-02?

    The 11-digit format is 55150023202. 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 5-3-2 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
    5-3-255150-232-025-4-255150-0232-02