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.
| Drug | Products here | Companies listing it |
|---|---|---|
| Rivaroxaban | 43 | 24 |
| Apixaban | 18 | 8 |
| Fondaparinux sodium | 28 | 6 |
| Edoxaban tosylate | 3 | 1 |
| Rivaroxaban granule | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 8 | tablet, film coated | New drug applications (NDA) | December 28, 2012 |
| Mylan Institutional LLC | 8 | injection, solution | New drug applications (NDA) | January 5, 2015 |
| Indoco Remedies Limited | 6 | tablet, film coated | Generic drugs (ANDA) | August 11, 2025 |
| Janssen Pharmaceuticals, Inc. | 5 | tablet, film coated; granule, for suspension | New drug applications (NDA) | December 1, 2021 |
| Alembic Pharmaceuticals Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | May 14, 2025 |
| Alembic Pharmaceuticals Limited | 4 | tablet, film coated | Generic drugs (ANDA) | May 14, 2025 |
| Cardinal Health 107, LLC | 4 | tablet, film coated | New drug applications (NDA) | December 28, 2012 |
| Dr. Reddy's Laboratories Limited | 4 | injection | Generic drugs (ANDA) | July 14, 2011 |
| E.r. Squibb & Sons, L.L.C. | 4 | tablet, film coated; tablet, for suspension | New drug applications (NDA) | September 15, 2025 |
| Eugia US LLC | 4 | injection, solution | Generic drugs (ANDA) | December 26, 2017 |
| Italfarmaco SpA | 4 | injection, solution | Generic drugs (ANDA) | February 6, 2019 |
| Sandoz Inc | 4 | injection | Generic drugs (ANDA) | June 18, 2019 |
| Zydus Pharmaceuticals USA Inc. | 4 | injection, solution | Generic drugs (ANDA) | February 6, 2019 |
| Aphena Pharma Solutions - Tennessee, LLC | 3 | tablet, film coated | New drug applications (NDA) | December 28, 2012 |
| Changzhou Pharmaceutical Factory | 3 | tablet, film coated | Generic drugs (ANDA) | February 1, 2026 |
| Daiichi Sankyo Inc. | 3 | tablet, film coated | New drug applications (NDA) | January 12, 2015 |
| Amneal Pharmaceuticals of New York LLC | 2 | tablet, film coated | Generic drugs (ANDA) | August 31, 2018 |
| Apotex Corp. | 1 | tablet, film coated | Generic drugs (ANDA) | May 2, 2025 |
| Ascend Laboratories, LLC | 1 | granule, for suspension | Generic drugs (ANDA) | July 7, 2025 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | April 10, 2025 |
| Camber Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 20, 2025 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet | Generic drugs (ANDA) | May 14, 2025 |
| Exelan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2025 |
| Florida Pharmaceutical Products, LLC | 1 | tablet | Generic drugs (ANDA) | August 20, 2025 |
| Lifestar Pharma LLC | 1 | tablet | Generic drugs (ANDA) | October 1, 2026 |
| Lupin Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 6, 2025 |
| Lupin Pharmaceuticals, Inc. | 1 | for suspension | Generic drugs (ANDA) | September 29, 2025 |
| Macleods Pharmaceuticals Limited | 1 | tablet, film coated | Generic drugs (ANDA) | May 14, 2025 |
| Micro Labs Limited | 1 | tablet | Generic drugs (ANDA) | July 6, 2026 |
| NorthStar RxLLC | 1 | tablet, film coated | Generic drugs (ANDA) | June 4, 2026 |
| Novadoz Pharmaceuticals LLC | 1 | tablet, film coated | Generic drugs (ANDA) | October 24, 2025 |
| Proficient Rx LP | 1 | tablet, film coated | New drug applications (NDA) | December 28, 2012 |
| Remedyrepack Inc. | 1 | tablet, film coated | New drug applications (NDA) | August 29, 2025 |
| ScieGen Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2025 |
| Sun Pharmaceutical Industries, Inc. | 1 | tablet, coated | Generic drugs (ANDA) | October 15, 2025 |
| XLCare Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | December 17, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 55 | 59.1% |
| Injection, solution | 20 | 21.5% |
| Injection | 8 | 8.6% |
| Tablet | 4 | 4.3% |
| Granule, for suspension | 2 | 2.2% |
| Tablet, for suspension | 1 | 1.1% |
| Capsule | 1 | 1.1% |
| Tablet, coated | 1 | 1.1% |
| For suspension | 1 | 1.1% |
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.