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Data / Drug companies / Donepezil hydrochloride

Donepezil hydrochloride: 34 companies and 73 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Donepezil hydrochloride is listed in the FDA National Drug Code Directory by 34 companies, with 73 products in commercial distribution. 70 of the products (95.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; tablet, orally disintegrating, and the newest product started marketing on August 20, 2025.

The request: Get every company that lists donepezil hydrochloride in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
34
Products
73
Generic (ANDA) products
70 (95.9%)
Application numbers
20
Routes
Oral
Brand names
Donepezil, Aricept
openFDA record search
api.fda.gov

Companies that list donepezil hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack5tablet, film coatedGeneric drugs (ANDA)August 17, 2012
Macleods Pharmaceuticals Limited5tablet, film coated; tablet, orally disintegratingGeneric drugs (ANDA)January 23, 2014
A-S Medication Solutions4tablet, film coated; tabletGeneric drugs (ANDA)February 2, 2015
Solco Healthcare US, LLC4tablet, film coatedGeneric drugs (ANDA)November 1, 2011
Unichem Pharmaceuticals (USA), Inc.4tablet, orally disintegrating; tablet, film coatedGeneric drugs (ANDA)November 10, 2016
Eisai Inc.3tablet, film coatedNew drug applications (NDA)July 23, 2010
Remedyrepack Inc.3tablet, film coated; tabletGeneric drugs (ANDA)July 15, 2025
Alembic Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)January 29, 2016
Alembic Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)January 29, 2016
American Health Packaging2tabletGeneric drugs (ANDA)May 17, 2017
Asclemed USA Inc.2tablet, film coatedGeneric drugs (ANDA)November 1, 2011
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)May 31, 2011
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)March 1, 2015
Cadila Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)January 30, 2017
Camber Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)February 2, 2015
Cardinal Health 107, LLC2tablet, film coatedGeneric drugs (ANDA)May 28, 2011
Direct_Rx2tablet, film coatedGeneric drugs (ANDA)September 3, 2021
Golden State Medical Supply, Inc.2tablet, film coatedGeneric drugs (ANDA)October 29, 2014
Major Pharmaceuticals2tablet, film coatedGeneric drugs (ANDA)May 28, 2011
NCS HealthCare of Ky, LLC DBA Vangard Labs2tablet, film coatedGeneric drugs (ANDA)August 17, 2012
Preferred Pharmaceuticals Inc.2tablet; tablet, film coatedGeneric drugs (ANDA)July 8, 2024
Quallent Pharmaceuticals Health LLC2tabletGeneric drugs (ANDA)July 19, 2023
Rising Pharma Holdings, Inc.2tablet, film coatedGeneric drugs (ANDA)May 31, 2011
ScieGen Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)October 29, 2014
Torrent Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)May 31, 2011
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)March 1, 2015
Coupler LLC1tablet, film coatedGeneric drugs (ANDA)January 31, 2025
Dr. Reddy's Laboratories Limited1tablet, film coatedGeneric drugs (ANDA)August 20, 2025
Edenbridge Pharmaceuticals LLC.1tablet, film coatedGeneric drugs (ANDA)February 19, 2016
Golden State Medical Supply, Inc.1tablet, film coatedGeneric drugs (ANDA)October 29, 2014
Lupin Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)December 21, 2015
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)March 1, 2015
Sun Pharmaceutical Industries, Inc.1tablet, film coatedGeneric drugs (ANDA)June 17, 2015
Upsher-Smith Laboratories, LLC1tablet, film coatedGeneric drugs (ANDA)March 1, 2015

Dosage forms

Dosage formProductsShare
Tablet, film coated5980.8%
Tablet1013.7%
Tablet, orally disintegrating45.5%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)7095.9%
New drug applications (NDA)34.1%

Pharmacologic classes

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.