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Data / Drug companies / Divalproex sodium

Divalproex sodium: 48 companies and 195 products in the FDA NDC directory

Divalproex sodium is listed in the FDA National Drug Code Directory by 48 companies, with 195 products in commercial distribution. 173 of the products (88.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, delayed release; tablet, film coated, extended release; tablet, extended release, and the newest product started marketing on October 19, 2026.

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Companies listing it
48
Products
195
Generic (ANDA) products
173 (88.7%)
Application numbers
24
Routes
Oral
Brand names
Depakote, Depakote Er, Depakote Sprinkles
openFDA record search
api.fda.gov

Companies that list divalproex sodium

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Remedyrepack Inc.20tablet, delayed release; tablet, extended releaseGeneric drugs (ANDA)February 17, 2026
Hahnemann Laboratories, Inc.16pelletUnapproved homeopathic productsMarch 28, 2023
Bryant Ranch Prepack11tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)June 26, 2024
A-S Medication Solutions9tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)June 26, 2024
Aphena Pharma Solutions - Tennessee, LLC8tablet, film coated, extended release; tablet, delayed releaseGeneric drugs (ANDA)June 2, 2014
Coupler LLC8tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)October 19, 2026
BluePoint Laboratories7tablet, film coated, extended release; tablet, delayed releaseGeneric drugs (ANDA)June 6, 2025
Cardinal Health 107, LLC7tablet, delayed release; capsule, delayed releaseGeneric drugs (ANDA)October 7, 2026
NCS HealthCare of Ky, LLC DBA Vangard Labs7tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)June 26, 2024
AbbVie Inc.6tablet, delayed release; tablet, extended releaseNew drug applications (NDA)June 30, 2023
Dr. Reddy's Laboratories Limited6tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)August 11, 2013
American Health Packaging5tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)December 29, 2025
American Health Packaging5tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)January 26, 2016
Aurobindo Pharma Limited5tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)October 24, 2014
Lupin Pharmaceuticals, Inc.5tablet, delayed release; tablet, extended releaseGeneric drugs (ANDA)September 18, 2020
Major Pharmaceuticals5tablet, delayed release; tablet, extended releaseGeneric drugs (ANDA)June 1, 2015
Preferred Pharmaceuticals Inc.5tablet, delayed release; tablet, extended releaseGeneric drugs (ANDA)September 24, 2026
Unichem Pharmaceuticals (USA), Inc.5tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)February 25, 2022
Bryant Ranch Prepack4tablet, delayed release; tablet, film coated, extended releaseGeneric drugs (ANDA)June 2, 2014
Bionpharma Inc.3tablet, delayed releaseGeneric drugs (ANDA)June 26, 2024
PD-Rx Pharmaceuticals, Inc.3tablet, delayed release; tablet, extended releaseGeneric drugs (ANDA)September 18, 2020
Rising Pharma Holdings, Inc.3tablet, delayed releaseGeneric drugs (ANDA)October 24, 2014
Sun Pharmaceutical Industries, Inc.3tablet, delayed releaseGeneric drugs (ANDA)July 29, 2008
Upsher-Smith Laboratories, LLC3tablet, delayed releaseGeneric drugs (ANDA)March 21, 2014
Amneal Pharmaceuticals LLC2tablet, extended releaseGeneric drugs (ANDA)June 1, 2015
Atlantic Biologicals Corp.2capsule, coated pellets; tablet, delayed releaseGeneric drugs (ANDA)January 31, 2019
AvPAK2tablet, extended releaseGeneric drugs (ANDA)September 16, 2022
Bryant Ranch Prepack2tablet, film coated, extended release; tablet, delayed releaseGeneric drugs (ANDA)June 2, 2014
Camber Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)September 26, 2023
Mylan Institutional Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)February 3, 2009
Mylan Pharmaceuticals Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)February 2, 2009
NorthStar Rx LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)June 2, 2014
Proficient Rx LP2tablet, delayed releaseGeneric drugs (ANDA)October 1, 2011
Safecor Health, LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)February 24, 2026
St. Mary's Medical Park Pharmacy2tablet, delayed releaseGeneric drugs (ANDA)May 13, 2025
Unit Dose Solutions, Inc.2tablet, delayed releaseGeneric drugs (ANDA)June 17, 2026
Ajanta Pharma USA Inc.1capsule, coated pelletsGeneric drugs (ANDA)May 15, 2020
Alembic Pharmaceuticals Inc.1capsule, delayed releaseGeneric drugs (ANDA)December 23, 2024
Alembic Pharmaceuticals Limited1capsule, delayed releaseGeneric drugs (ANDA)December 23, 2024
Direct RX1tablet, delayed releaseGeneric drugs (ANDA)April 6, 2022
First Nation Group, LLC1capsule, coated pelletsGeneric drugs (ANDA)November 10, 2025
Lifestar Pharma LLC1capsule, coated pelletsGeneric drugs (ANDA)August 12, 2025
NorthStar RxLLC1capsule, delayed releaseGeneric drugs (ANDA)August 1, 2024
Northwind Health Company, LLC1tablet, delayed releaseGeneric drugs (ANDA)May 29, 2020
NuCare Pharmaceuticals,Inc.1tablet, delayed releaseGeneric drugs (ANDA)July 29, 2008
Proficient Rx LP1tablet, delayed releaseGeneric drugs (ANDA)June 26, 2024
Zydus Lifesciences Limited1capsule, coated pelletsGeneric drugs (ANDA)January 27, 2009
Zydus Pharmaceuticals USA Inc.1capsule, coated pelletsGeneric drugs (ANDA)January 27, 2009

Dosage forms

Dosage formProductsShare
Tablet, delayed release9146.7%
Tablet, film coated, extended release4925.1%
Tablet, extended release2110.8%
Pellet168.2%
Capsule, coated pellets105.1%
Capsule, delayed release63.1%
Capsule21%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)17388.7%
Unapproved homeopathic products168.2%
New drug applications (NDA)63.1%

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.