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Data / Drug companies / Factor Xa Inhibitor

Factor Xa Inhibitor drugs: 5 drugs from 36 companies in the FDA NDC directory

Factor Xa Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 93 products in this class from 36 companies, covering 5 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 1, 2026.

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  • 36Companies
  • 93Products
  • 5Drugs by generic name

Drugs in the Factor Xa Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Rivaroxaban4324
Apixaban188
Fondaparinux sodium286
Edoxaban tosylate31
Rivaroxaban granule11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions8tablet, film coatedNew drug applications (NDA)December 28, 2012
Mylan Institutional LLC8injection, solutionNew drug applications (NDA)January 5, 2015
Indoco Remedies Limited6tablet, film coatedGeneric drugs (ANDA)August 11, 2025
Janssen Pharmaceuticals, Inc.5tablet, film coated; granule, for suspensionNew drug applications (NDA)December 1, 2021
Alembic Pharmaceuticals Inc.4tablet, film coatedGeneric drugs (ANDA)May 14, 2025
Alembic Pharmaceuticals Limited4tablet, film coatedGeneric drugs (ANDA)May 14, 2025
Cardinal Health 107, LLC4tablet, film coatedNew drug applications (NDA)December 28, 2012
Dr. Reddy's Laboratories Limited4injectionGeneric drugs (ANDA)July 14, 2011
E.r. Squibb & Sons, L.L.C.4tablet, film coated; tablet, for suspensionNew drug applications (NDA)September 15, 2025
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
Aphena Pharma Solutions - Tennessee, LLC3tablet, film coatedNew drug applications (NDA)December 28, 2012
Changzhou Pharmaceutical Factory3tablet, film coatedGeneric drugs (ANDA)February 1, 2026
Daiichi Sankyo Inc.3tablet, film coatedNew drug applications (NDA)January 12, 2015
Amneal Pharmaceuticals of New York LLC2tablet, film coatedGeneric drugs (ANDA)August 31, 2018
Apotex Corp.1tablet, film coatedGeneric drugs (ANDA)May 2, 2025
Ascend Laboratories, LLC1granule, for suspensionGeneric drugs (ANDA)July 7, 2025
Aurobindo Pharma Limited1tablet, film coatedGeneric drugs (ANDA)April 10, 2025
Camber Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)May 20, 2025
Dr. Reddy's Laboratories Inc.1tabletGeneric drugs (ANDA)May 14, 2025
Exelan Pharmaceuticals Inc.1tablet, film coatedGeneric drugs (ANDA)August 4, 2025
Florida Pharmaceutical Products, LLC1tabletGeneric drugs (ANDA)August 20, 2025
Lifestar Pharma LLC1tabletGeneric drugs (ANDA)October 1, 2026
Lupin Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)March 6, 2025
Lupin Pharmaceuticals, Inc.1for suspensionGeneric drugs (ANDA)September 29, 2025
Macleods Pharmaceuticals Limited1tablet, film coatedGeneric drugs (ANDA)May 14, 2025
Micro Labs Limited1tabletGeneric drugs (ANDA)July 6, 2026
NorthStar RxLLC1tablet, film coatedGeneric drugs (ANDA)June 4, 2026
Novadoz Pharmaceuticals LLC1tablet, film coatedGeneric drugs (ANDA)October 24, 2025
Proficient Rx LP1tablet, film coatedNew drug applications (NDA)December 28, 2012
Remedyrepack Inc.1tablet, film coatedNew drug applications (NDA)August 29, 2025
ScieGen Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)August 4, 2025
Sun Pharmaceutical Industries, Inc.1tablet, coatedGeneric drugs (ANDA)October 15, 2025
XLCare Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)December 17, 2025

Dosage forms

Dosage formProductsShare
Tablet, film coated5559.1%
Injection, solution2021.5%
Injection88.6%
Tablet44.3%
Granule, for suspension22.2%
Tablet, for suspension11.1%
Capsule11.1%
Tablet, coated11.1%
For suspension11.1%

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.