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Data / Drug companies / Rivaroxaban

Rivaroxaban: 24 companies and 46 products in the FDA NDC directory

Rivaroxaban is listed in the FDA National Drug Code Directory by 24 companies, with 46 products in commercial distribution. 33 of the products (71.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; kit, and the newest product started marketing on October 1, 2026.

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Companies listing it
24
Products
46
Generic (ANDA) products
33 (71.7%)
Application numbers
17
Routes
Oral
Brand names
Xarelto, Xarelto
openFDA record search
api.fda.gov

Companies that list rivaroxaban

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Janssen Pharmaceuticals, Inc.6tablet, film coated; kitNew drug applications (NDA)December 1, 2021
Alembic Pharmaceuticals Inc.5tablet, film coated; kitGeneric drugs (ANDA)May 14, 2025
Alembic Pharmaceuticals Limited5tablet, film coated; kitGeneric drugs (ANDA)May 14, 2025
A-S Medication Solutions4tablet, film coatedNew drug applications (NDA)November 5, 2011
Indoco Remedies Limited4tablet, film coatedGeneric drugs (ANDA)August 11, 2025
Changzhou Pharmaceutical Factory3tablet, film coatedGeneric drugs (ANDA)February 1, 2026
Cardinal Health 107, LLC2tablet, film coatedNew drug applications (NDA)November 5, 2011
Aphena Pharma Solutions - Tennessee, LLC1tablet, film coatedNew drug applications (NDA)July 1, 2011
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
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
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 coated3678.3%
Tablet48.7%
Kit36.5%
Granule, for suspension24.3%
Tablet, coated12.2%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3371.7%
New drug applications (NDA)1328.3%

Pharmacologic classes

ClassProducts
Factor Xa Inhibitor43

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.