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Data / Drug companies / Fondaparinux sodium

Fondaparinux sodium: 6 companies and 28 products in the FDA NDC directory

Fondaparinux sodium is listed in the FDA National Drug Code Directory by 6 companies, with 28 products in commercial distribution. 20 of the products (71.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection, and the newest product started marketing on June 18, 2019.

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Companies listing it
6
Products
28
Generic (ANDA) products
20 (71.4%)
Application numbers
5
Routes
Subcutaneous
Brand names
Arixtra
openFDA record search
api.fda.gov

Companies that list fondaparinux sodium

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Mylan Institutional LLC8injection, solutionNew drug applications (NDA)January 5, 2015
Dr. Reddy's Laboratories Limited4injectionGeneric drugs (ANDA)July 14, 2011
Eugia US LLC4injection, solutionGeneric drugs (ANDA)December 26, 2017
Italfarmaco SpA4injection, solutionGeneric drugs (ANDA)February 6, 2019
Sandoz Inc4injectionGeneric drugs (ANDA)June 18, 2019
Zydus Pharmaceuticals USA Inc.4injection, solutionGeneric drugs (ANDA)February 6, 2019

Dosage forms

Dosage formProductsShare
Injection, solution2071.4%
Injection828.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2071.4%
New drug applications (NDA)414.3%
Authorized generics (NDA)414.3%

Pharmacologic classes

ClassProducts
Factor Xa Inhibitor28

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.