Fondaparinux Sodium Injection, Solution
NDC Package 11797-155-06
Package Information
Fondaparinux Sodium injection is fondaparinux is used to treat serious blood clots in the legs and/or lungs. This formulation utilizes a injection, solution delivery system. Marketed by Italfarmaco S.p.a, this product is identified by NDC 11797-155 and is authorized under FDA application ANDA208615.
Identification & Billing
- 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
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 11797 - Italfarmaco S.p.a
- 11797-155 - Fondaparinux Sodium
- 11797-155-06 - 10 SYRINGE in 1 CARTON / .4 mL in 1 SYRINGE (11797-155-02)
- 11797-155 - Fondaparinux Sodium
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (11797-155). Click a package code to view its specific billing and regulatory data.
* 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 11797-155-06 identifies a specific commercial package of 10 syringe in 1 carton / .4 ml in 1 syringe (11797-155-02) of Fondaparinux Sodium, a human prescription drug labeled by Italfarmaco S.p.a. This injection, solution is formulated for subcutaneous 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 Italfarmaco S.p.a on February 06, 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 Italfarmaco S.p.a product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 11797015506. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.