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.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Remedyrepack Inc. | 20 | tablet, delayed release; tablet, extended release | Generic drugs (ANDA) | February 17, 2026 |
| Hahnemann Laboratories, Inc. | 16 | pellet | Unapproved homeopathic products | March 28, 2023 |
| Bryant Ranch Prepack | 11 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | June 26, 2024 |
| A-S Medication Solutions | 9 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | June 26, 2024 |
| Aphena Pharma Solutions - Tennessee, LLC | 8 | tablet, film coated, extended release; tablet, delayed release | Generic drugs (ANDA) | June 2, 2014 |
| Coupler LLC | 8 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | October 19, 2026 |
| BluePoint Laboratories | 7 | tablet, film coated, extended release; tablet, delayed release | Generic drugs (ANDA) | June 6, 2025 |
| Cardinal Health 107, LLC | 7 | tablet, delayed release; capsule, delayed release | Generic drugs (ANDA) | October 7, 2026 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 7 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | June 26, 2024 |
| AbbVie Inc. | 6 | tablet, delayed release; tablet, extended release | New drug applications (NDA) | June 30, 2023 |
| Dr. Reddy's Laboratories Limited | 6 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | August 11, 2013 |
| American Health Packaging | 5 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | December 29, 2025 |
| American Health Packaging | 5 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | January 26, 2016 |
| Aurobindo Pharma Limited | 5 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | October 24, 2014 |
| Lupin Pharmaceuticals, Inc. | 5 | tablet, delayed release; tablet, extended release | Generic drugs (ANDA) | September 18, 2020 |
| Major Pharmaceuticals | 5 | tablet, delayed release; tablet, extended release | Generic drugs (ANDA) | June 1, 2015 |
| Preferred Pharmaceuticals Inc. | 5 | tablet, delayed release; tablet, extended release | Generic drugs (ANDA) | September 24, 2026 |
| Unichem Pharmaceuticals (USA), Inc. | 5 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | February 25, 2022 |
| Bryant Ranch Prepack | 4 | tablet, delayed release; tablet, film coated, extended release | Generic drugs (ANDA) | June 2, 2014 |
| Bionpharma Inc. | 3 | tablet, delayed release | Generic drugs (ANDA) | June 26, 2024 |
| PD-Rx Pharmaceuticals, Inc. | 3 | tablet, delayed release; tablet, extended release | Generic drugs (ANDA) | September 18, 2020 |
| Rising Pharma Holdings, Inc. | 3 | tablet, delayed release | Generic drugs (ANDA) | October 24, 2014 |
| Sun Pharmaceutical Industries, Inc. | 3 | tablet, delayed release | Generic drugs (ANDA) | July 29, 2008 |
| Upsher-Smith Laboratories, LLC | 3 | tablet, delayed release | Generic drugs (ANDA) | March 21, 2014 |
| Amneal Pharmaceuticals LLC | 2 | tablet, extended release | Generic drugs (ANDA) | June 1, 2015 |
| Atlantic Biologicals Corp. | 2 | capsule, coated pellets; tablet, delayed release | Generic drugs (ANDA) | January 31, 2019 |
| AvPAK | 2 | tablet, extended release | Generic drugs (ANDA) | September 16, 2022 |
| Bryant Ranch Prepack | 2 | tablet, film coated, extended release; tablet, delayed release | Generic drugs (ANDA) | June 2, 2014 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | September 26, 2023 |
| Mylan Institutional Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | February 3, 2009 |
| Mylan Pharmaceuticals Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | February 2, 2009 |
| NorthStar Rx LLC | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | June 2, 2014 |
| Proficient Rx LP | 2 | tablet, delayed release | Generic drugs (ANDA) | October 1, 2011 |
| Safecor Health, LLC | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | February 24, 2026 |
| St. Mary's Medical Park Pharmacy | 2 | tablet, delayed release | Generic drugs (ANDA) | May 13, 2025 |
| Unit Dose Solutions, Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | June 17, 2026 |
| Ajanta Pharma USA Inc. | 1 | capsule, coated pellets | Generic drugs (ANDA) | May 15, 2020 |
| Alembic Pharmaceuticals Inc. | 1 | capsule, delayed release | Generic drugs (ANDA) | December 23, 2024 |
| Alembic Pharmaceuticals Limited | 1 | capsule, delayed release | Generic drugs (ANDA) | December 23, 2024 |
| Direct RX | 1 | tablet, delayed release | Generic drugs (ANDA) | April 6, 2022 |
| First Nation Group, LLC | 1 | capsule, coated pellets | Generic drugs (ANDA) | November 10, 2025 |
| Lifestar Pharma LLC | 1 | capsule, coated pellets | Generic drugs (ANDA) | August 12, 2025 |
| NorthStar RxLLC | 1 | capsule, delayed release | Generic drugs (ANDA) | August 1, 2024 |
| Northwind Health Company, LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | May 29, 2020 |
| NuCare Pharmaceuticals,Inc. | 1 | tablet, delayed release | Generic drugs (ANDA) | July 29, 2008 |
| Proficient Rx LP | 1 | tablet, delayed release | Generic drugs (ANDA) | June 26, 2024 |
| Zydus Lifesciences Limited | 1 | capsule, coated pellets | Generic drugs (ANDA) | January 27, 2009 |
| Zydus Pharmaceuticals USA Inc. | 1 | capsule, coated pellets | Generic drugs (ANDA) | January 27, 2009 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, delayed release | 91 | 46.7% |
| Tablet, film coated, extended release | 49 | 25.1% |
| Tablet, extended release | 21 | 10.8% |
| Pellet | 16 | 8.2% |
| Capsule, coated pellets | 10 | 5.1% |
| Capsule, delayed release | 6 | 3.1% |
| Capsule | 2 | 1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 173 | 88.7% |
| Unapproved homeopathic products | 16 | 8.2% |
| New drug applications (NDA) | 6 | 3.1% |
Pharmacologic classes
| Class | Products |
|---|---|
| Anti-epileptic Agent | 195 |
| Mood Stabilizer | 195 |
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.