Data / Drug companies / Paroxetine
Paroxetine: 33 companies and 83 products in the FDA NDC directory
Paroxetine is listed in the FDA National Drug Code Directory by 33 companies, with 83 products in commercial distribution. 81 of the products (97.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, film coated, extended release; capsule, and the newest product started marketing on August 21, 2026.
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- Companies listing it
- 33
- Products
- 83
- Generic (ANDA) products
- 81 (97.6%)
- Application numbers
- 12
- Routes
- Oral
- Brand names
- Brisdelle
- openFDA record search
- api.fda.gov
Companies that list paroxetine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Chartwell RX, LLC | 7 | tablet, film coated; tablet, film coated, extended release | Generic drugs (ANDA) | November 2, 2021 |
| Remedyrepack Inc. | 5 | tablet, film coated | Generic drugs (ANDA) | September 13, 2022 |
| American Health Packaging | 4 | tablet, film coated | Generic drugs (ANDA) | March 15, 2005 |
| Asclemed USA, Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Aurolife Pharma, LLC | 4 | tablet, film coated | Generic drugs (ANDA) | December 3, 2009 |
| Proficient Rx LP | 4 | tablet, film coated | Generic drugs (ANDA) | December 3, 2009 |
| Yiling Pharmaceutical, Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | November 2, 2021 |
| Zydus Pharmaceuticals USA Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Alembic Pharmaceuticals Inc. | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | March 31, 2026 |
| Alembic Pharmaceuticals Limited | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | March 31, 2026 |
| AvPAK | 3 | tablet, film coated | Generic drugs (ANDA) | March 11, 2016 |
| Cadila Pharmaceuticals Limited | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | February 14, 2020 |
| Lupin Pharmaceuticals, Inc. | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | March 6, 2017 |
| Modavar Pharmaceuticals LLC | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | October 20, 2021 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 3 | tablet, film coated | Generic drugs (ANDA) | November 1, 2014 |
| Westminster Pharmaceuticals, LLC | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | July 26, 2021 |
| A-S Medication Solutions | 2 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Coupler LLC | 2 | tablet, film coated | Generic drugs (ANDA) | August 21, 2026 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Preferred Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 6, 2018 |
| Advanced Rx of Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | May 19, 2023 |
| Ani Pharmaceuticals, Inc. | 1 | suspension | Generic drugs (ANDA) | September 3, 2021 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 3, 2009 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 3, 2009 |
| Direct RX | 1 | tablet, film coated | Generic drugs (ANDA) | February 29, 2016 |
| Direct_Rx | 1 | tablet, film coated | Generic drugs (ANDA) | June 21, 2023 |
| Hawaii Repack, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Legacy Pharma USA Inc. | 1 | capsule | New drug applications (NDA) | February 18, 2025 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 13, 2007 |
| Padagis US LLC | 1 | capsule | Authorized generics (NDA) | October 3, 2017 |
| Solco Healthcare US, LLC | 1 | capsule | Generic drugs (ANDA) | August 15, 2017 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 58 | 69.9% |
| Tablet, film coated, extended release | 21 | 25.3% |
| Capsule | 3 | 3.6% |
| Suspension | 1 | 1.2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 81 | 97.6% |
| Authorized generics (NDA) | 1 | 1.2% |
| New drug applications (NDA) | 1 | 1.2% |
Pharmacologic classes
| Class | Products |
|---|---|
| Serotonin Reuptake Inhibitor | 83 |
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.