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Data / Drug companies / Memantine hydrochloride

Memantine hydrochloride: 36 companies and 104 products in the FDA NDC directory

Memantine hydrochloride is listed in the FDA National Drug Code Directory by 36 companies, with 104 products in commercial distribution. 98 of the products (94.2%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; capsule, extended release; tablet, film coated, and the newest product started marketing on August 28, 2025.

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Companies listing it
36
Products
104
Generic (ANDA) products
98 (94.2%)
Application numbers
23
Routes
Oral
Brand names
Memantine
openFDA record search
api.fda.gov

Companies that list memantine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions7tablet; tablet, film coatedGeneric drugs (ANDA)September 26, 2022
Macleods Pharmaceuticals Limited7capsule, extended release; tabletGeneric drugs (ANDA)August 28, 2025
Lupin Pharmaceuticals, Inc.6capsule, extended release; tablet, film coatedGeneric drugs (ANDA)February 20, 2018
Zydus Lifesciences Limited6capsule, extended release; tablet, film coatedGeneric drugs (ANDA)April 8, 2018
Aurobindo Pharma Limited5capsule, extended release; kitGeneric drugs (ANDA)August 9, 2021
Bryant Ranch Prepack5tablet; tablet, film coatedGeneric drugs (ANDA)February 28, 2019
Amneal Pharmaceuticals LLC4capsule, extended releaseGeneric drugs (ANDA)December 22, 2017
Aphena Pharma Solutions - Tennessee, LLC4tablet; tablet, film coatedGeneric drugs (ANDA)February 28, 2019
Bryant Ranch Prepack4tabletGeneric drugs (ANDA)February 28, 2019
Cardinal Health 107, LLC4tablet, film coated; tabletGeneric drugs (ANDA)July 20, 2015
Slate Run Pharmaceuticals, LLC4capsule, extended releaseGeneric drugs (ANDA)November 15, 2021
Vitruvias Therapeutics4capsule, extended releaseGeneric drugs (ANDA)February 19, 2024
Zydus Pharmaceuticals USA Inc.4capsule, extended releaseGeneric drugs (ANDA)April 8, 2018
Actavis Pharma, Inc.3tablet; kitAuthorized generics (NDA)April 1, 2015
Major Pharmaceuticals3tablet, film coated; capsule, extended releaseGeneric drugs (ANDA)February 20, 2018
Ajanta Pharma USA Inc.2tabletGeneric drugs (ANDA)August 27, 2015
Alembic Pharmaceuticals Inc.2tablet, coatedGeneric drugs (ANDA)October 13, 2015
Alembic Pharmaceuticals Limited2tablet, coatedGeneric drugs (ANDA)October 13, 2015
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)October 13, 2015
AvPAK2tablet, film coatedGeneric drugs (ANDA)February 20, 2024
Bryant Ranch Prepack2tabletGeneric drugs (ANDA)February 28, 2019
Camber Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)September 26, 2022
Carlsbad Technology, Inc.2tablet, film coatedGeneric drugs (ANDA)June 22, 2025
Dr. Reddy's Laboratories Limited2tablet, film coatedGeneric drugs (ANDA)July 11, 2015
Sun Pharmaceutical Industries, Inc.2tablet, film coatedGeneric drugs (ANDA)July 11, 2015
Unichem Pharmaceuticals (USA), Inc.2tablet, film coatedGeneric drugs (ANDA)November 1, 2015
Upsher-Smith Laboratories, LLC2tablet, film coatedGeneric drugs (ANDA)July 31, 2015
Viona Pharmaceuticals Inc2tabletGeneric drugs (ANDA)February 28, 2019
Apotex Corp.1solutionGeneric drugs (ANDA)April 30, 2018
Chartwell Governmental & Specialty RX, LLC.1solutionGeneric drugs (ANDA)October 13, 2015
Chartwell RX, LLC1solutionGeneric drugs (ANDA)October 13, 2015
Coupler LLC1tabletGeneric drugs (ANDA)February 4, 2025
Direct_Rx1tabletGeneric drugs (ANDA)November 11, 2021
NCS HealthCare of Ky, LLC DBA Vangard Labs1capsule, extended releaseGeneric drugs (ANDA)August 9, 2021
Preferred Pharmaceuticals Inc.1tabletGeneric drugs (ANDA)May 1, 2024
Remedyrepack Inc.1tabletGeneric drugs (ANDA)January 20, 2022

Dosage forms

Dosage formProductsShare
Tablet3432.7%
Capsule, extended release3432.7%
Tablet, film coated2625%
Tablet, coated43.8%
Solution43.8%
Kit21.9%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)9894.2%
Authorized generics (NDA)54.8%
New drug applications (NDA)11%

Pharmacologic classes

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.