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Data / Drug companies / Guanfacine

Guanfacine: 33 companies and 101 products in the FDA NDC directory

Guanfacine is listed in the FDA National Drug Code Directory by 33 companies, with 101 products in commercial distribution. 97 of the products (96.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, extended release; tablet, and the newest product started marketing on October 2, 2026.

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Companies listing it
33
Products
101
Generic (ANDA) products
97 (96.0%)
Application numbers
16
Routes
Oral
Brand names
Intuniv
openFDA record search
api.fda.gov

Companies that list guanfacine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Remedyrepack Inc.7tablet, extended release; tabletGeneric drugs (ANDA)June 2, 2026
Advagen Pharma Ltd6tablet, extended release; tabletGeneric drugs (ANDA)April 15, 2025
Upsher-Smith Laboratories, LLC6tablet, extended release; tabletGeneric drugs (ANDA)September 1, 2022
Bryant Ranch Prepack5tablet, extended releaseGeneric drugs (ANDA)August 8, 2023
A-S Medication Solutions4tablet, extended release; tabletGeneric drugs (ANDA)August 8, 2023
Actavis Pharma, Inc.4tablet, extended releaseGeneric drugs (ANDA)December 1, 2014
Alembic Pharmaceuticals Inc.4tablet, extended releaseGeneric drugs (ANDA)August 8, 2023
Alembic Pharmaceuticals Limited4tablet, extended releaseGeneric drugs (ANDA)August 8, 2023
Apotex Corp.4tablet, extended releaseGeneric drugs (ANDA)October 3, 2018
Fosun Pharma USA Inc.4tablet, extended releaseGeneric drugs (ANDA)April 3, 2026
Golden State Medical Supply, Inc.4tablet, extended releaseGeneric drugs (ANDA)August 7, 2023
NorthStar Rx LLC4tablet, extended releaseGeneric drugs (ANDA)September 17, 2021
Proficient Rx LP4tablet, extended releaseGeneric drugs (ANDA)July 7, 2017
Slate Run Pharmaceuticals, LLC4tablet, extended releaseGeneric drugs (ANDA)August 1, 2022
Takeda Pharmaceuticals America, Inc.4tablet, extended releaseNew drug applications (NDA)September 2, 2009
Unichem Pharmaceuticals (USA), Inc.4tablet, extended releaseGeneric drugs (ANDA)November 19, 2024
Bryant Ranch Prepack3tablet, extended releaseGeneric drugs (ANDA)August 17, 2018
Golden State Medical Supply, Inc.3tablet, extended releaseGeneric drugs (ANDA)June 2, 2015
Actavis Pharma, Inc.2tabletGeneric drugs (ANDA)October 17, 1995
Ajanta Pharma USA Inc.2tabletGeneric drugs (ANDA)April 27, 2023
Amneal Pharmaceuticals LLC2tabletGeneric drugs (ANDA)November 25, 1998
Amneal Pharmaceuticals of New York LLC2tabletGeneric drugs (ANDA)April 15, 2022
Bryant Ranch Prepack2tablet, extended releaseGeneric drugs (ANDA)August 17, 2018
Chartwell RX, LLC2tabletGeneric drugs (ANDA)September 1, 2022
Coupler LLC2tabletGeneric drugs (ANDA)January 28, 2026
Epic Pharma, LLC2tabletGeneric drugs (ANDA)December 2, 2013
AvPAK1tabletGeneric drugs (ANDA)June 7, 2017
Direct_Rx1tablet, extended releaseGeneric drugs (ANDA)October 2, 2026
Major Pharmaceuticals1tabletGeneric drugs (ANDA)December 2, 2013
Precision Dose, Inc.1tabletGeneric drugs (ANDA)January 31, 2023
Proficient Rx LP1tabletGeneric drugs (ANDA)December 2, 2013
Puracap Laboratories LLC DBA Blu Pharmaceuticals1tabletGeneric drugs (ANDA)November 14, 2016
St. Mary's Medical Park Pharmacy1tablet, extended releaseGeneric drugs (ANDA)May 19, 2025

Dosage forms

Dosage formProductsShare
Tablet, extended release7574.3%
Tablet2625.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)9796%
New drug applications (NDA)44%

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.