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Data / Drug companies / Topiramate

Topiramate: 56 companies and 303 products in the FDA NDC directory

Topiramate is listed in the FDA National Drug Code Directory by 56 companies, with 303 products in commercial distribution. 282 of the products (93.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; capsule, extended release; tablet, and the newest product started marketing on October 15, 2026.

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Companies listing it
56
Products
303
Generic (ANDA) products
282 (93.1%)
Application numbers
33
Routes
Oral
Brand names
Topamax, Qudexy XR, Trokendi XR, Eprontia
openFDA record search
api.fda.gov

Companies that list topiramate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Remedyrepack Inc.16tablet, film coated; tabletGeneric drugs (ANDA)November 4, 2025
A-S Medication Solutions13tablet, film coated; tabletGeneric drugs (ANDA)June 12, 2014
Bryant Ranch Prepack13tablet, film coated; tabletGeneric drugs (ANDA)December 15, 2014
Proficient Rx LP12tablet, film coated; tabletGeneric drugs (ANDA)December 15, 2014
Glenmark Pharmaceuticals Inc., USA11capsule, extended release; tablet, film coatedGeneric drugs (ANDA)July 16, 2024
Zydus Pharmaceuticals USA Inc.11tablet, film coated; capsule, extended releaseGeneric drugs (ANDA)October 24, 2024
Advanced Rx of Tennessee, LLC10tablet, film coated; tabletGeneric drugs (ANDA)February 18, 2026
Ajanta Pharma USA Inc.9capsule, extended releaseGeneric drugs (ANDA)September 2, 2025
Zydus Lifesciences Limited9capsule, extended releaseGeneric drugs (ANDA)November 13, 2023
Ascend Laboratories, LLC8capsule, extended release; capsuleGeneric drugs (ANDA)October 15, 2026
Camber Pharmaceuticals, Inc.8tablet; capsule, extended releaseGeneric drugs (ANDA)April 1, 2026
Cipla USA Inc.8tabletGeneric drugs (ANDA)July 22, 2016
Preferred Pharmaceuticals Inc.8tablet, film coatedGeneric drugs (ANDA)January 28, 2026
Zydus Lifesciences Limited7tablet, film coated; capsule, coated pelletsGeneric drugs (ANDA)October 24, 2024
Coupler LLC6tablet, film coated; tabletGeneric drugs (ANDA)August 26, 2026
Janssen Pharmaceuticals, Inc.6tablet, coated; capsule, coated pelletsNew drug applications (NDA)November 1, 1998
NuCare Pharmaceuticals,Inc.6tablet, film coated; tabletGeneric drugs (ANDA)December 15, 2014
Proficient Rx LP6tablet, film coatedGeneric drugs (ANDA)December 15, 2014
Cranbury Pharmaceuticals, LLC5capsule, extended releaseGeneric drugs (ANDA)October 1, 2026
NorthStar RxLLC5capsule, extended releaseGeneric drugs (ANDA)January 1, 2023
Northwind Health Company, LLC5tablet, film coated; tabletGeneric drugs (ANDA)February 6, 2023
PD-Rx Pharmaceuticals, Inc.5tablet; tablet, film coatedGeneric drugs (ANDA)December 15, 2014
Upsher-Smith Laboratories, LLC5capsule, extended releaseAuthorized generics (NDA)July 7, 2014
Upsher-Smith Laboratories, LLC5capsule, extended releaseNew drug applications (NDA)April 11, 2014
Vitruvias Therapeutics5capsule, extended releaseGeneric drugs (ANDA)April 7, 2025
Zydus Pharmaceuticals USA Inc.5capsule, extended releaseGeneric drugs (ANDA)January 17, 2023
American Health Packaging4tablet, film coatedGeneric drugs (ANDA)November 8, 2019
Aphena Pharma Solutions - Tennessee, LLC4tabletGeneric drugs (ANDA)September 7, 2020
Asclemed USA, Inc.4tabletGeneric drugs (ANDA)June 12, 2014
Aurobindo Pharma Limited4tablet, film coatedGeneric drugs (ANDA)March 27, 2009
AvKARE4capsule, extended releaseGeneric drugs (ANDA)October 30, 2024
AvPAK4tablet, film coatedGeneric drugs (ANDA)June 8, 2026
Bryant Ranch Prepack4tablet, film coatedGeneric drugs (ANDA)July 1, 2013
Dr. Reddy's Laboratories Inc.4capsule, extended releaseGeneric drugs (ANDA)February 1, 2026
Exelan Pharmaceuticals Inc.4tabletGeneric drugs (ANDA)September 7, 2020
Lupin Pharmaceuticals, Inc.4capsule, extended releaseGeneric drugs (ANDA)February 3, 2026
Par Health USA, LLC4capsule, extended releaseGeneric drugs (ANDA)May 26, 2023
St. Mary's Medical Park Pharmacy4tablet, film coatedGeneric drugs (ANDA)September 17, 2026
Sun Pharmaceutical Industries, Inc.4tablet, film coatedGeneric drugs (ANDA)March 27, 2009
Sun Pharmaceutical Industries, Inc.4tablet, film coatedGeneric drugs (ANDA)December 15, 2014
Supernus Pharmaceuticals, Inc.4capsule, extended releaseNew drug applications (NDA)August 16, 2013
Teva Pharmaceuticals, Inc.4capsule, extended releaseGeneric drugs (ANDA)May 3, 2023
Unichem Pharmaceuticals (USA), Inc.4tablet, film coatedGeneric drugs (ANDA)July 1, 2013
XLCare Pharmaceuticals, Inc.4tabletGeneric drugs (ANDA)July 10, 2025
Advagen Pharma Ltd3capsuleGeneric drugs (ANDA)May 27, 2025
NCS HealthCare of Ky, LLC DBA Vangard Labs3tablet, film coatedGeneric drugs (ANDA)March 27, 2009
PD-Rx Pharmaceuticals, Inc.3tablet, film coatedGeneric drugs (ANDA)December 15, 2014
Quallent Pharmaceuticals Health LLC3tablet, film coatedGeneric drugs (ANDA)July 24, 2023
Aurobindo Pharma Limited2capsuleGeneric drugs (ANDA)September 27, 2023
Cardinal Health 107, LLC2tablet, film coatedGeneric drugs (ANDA)June 1, 2012
Major Pharmaceuticals2tablet, film coatedGeneric drugs (ANDA)March 27, 2009
Upsher-Smith Laboratories, LLC2capsuleGeneric drugs (ANDA)December 5, 2023
Azurity Pharmaceuticals, Inc.1solutionNew drug applications (NDA)December 6, 2021
Direct RX1tabletGeneric drugs (ANDA)April 17, 2024
Kesin Pharma Corporation1solutionGeneric drugs (ANDA)July 7, 2025
Unit Dose Solutions, Inc.1tablet, film coatedGeneric drugs (ANDA)July 9, 2026

Dosage forms

Dosage formProductsShare
Tablet, film coated12942.6%
Capsule, extended release8929.4%
Tablet5718.8%
Capsule, coated pellets113.6%
Capsule93%
Solution41.3%
Tablet, coated41.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)28293.1%
New drug applications (NDA)165.3%
Authorized generics (NDA)51.7%

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.