Data / Drug companies / Fluoxetine
Fluoxetine: 42 companies and 95 products in the FDA NDC directory
Fluoxetine is listed in the FDA National Drug Code Directory by 42 companies, with 95 products in commercial distribution. 95 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; tablet, film coated; tablet, and the newest product started marketing on October 2, 2026.
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- Companies listing it
- 42
- Products
- 95
- Generic (ANDA) products
- 95 (100.0%)
- Application numbers
- 18
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list fluoxetine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 7 | capsule; tablet, film coated | Generic drugs (ANDA) | July 11, 2025 |
| Remedyrepack Inc. | 7 | capsule; tablet, film coated | Generic drugs (ANDA) | April 23, 2026 |
| Aurobindo Pharma Limited | 6 | capsule; tablet, film coated | Generic drugs (ANDA) | July 11, 2025 |
| Alembic Pharmaceuticals Inc. | 5 | capsule; tablet, film coated | Generic drugs (ANDA) | April 7, 2017 |
| A-S Medication Solutions | 4 | capsule | Generic drugs (ANDA) | September 1, 2025 |
| Alembic Pharmaceuticals Limited | 3 | capsule | Generic drugs (ANDA) | July 1, 2009 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | January 15, 2026 |
| BluePoint Laboratories | 3 | capsule | Generic drugs (ANDA) | January 8, 2026 |
| Cadila Pharmaceuticals Limited | 3 | capsule | Generic drugs (ANDA) | December 15, 2022 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 3 | capsule | Generic drugs (ANDA) | October 13, 2024 |
| Modavar Pharmaceuticals LLC | 3 | capsule | Generic drugs (ANDA) | September 8, 2021 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 3 | capsule | Generic drugs (ANDA) | July 11, 2025 |
| NorthStar RxLLC | 3 | capsule | Generic drugs (ANDA) | September 1, 2025 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | November 16, 2017 |
| Coupler LLC | 2 | capsule | Generic drugs (ANDA) | October 2, 2026 |
| Legacy Pharmaceutical Packaging, LLC | 2 | capsule | Generic drugs (ANDA) | January 25, 2011 |
| NorthStar Rx LLC | 2 | tablet, film coated | Generic drugs (ANDA) | September 18, 2019 |
| Northwind Health Company, LLC | 2 | capsule | Generic drugs (ANDA) | April 21, 2026 |
| NuCare Pharmaceuticals,Inc. | 2 | capsule | Generic drugs (ANDA) | January 29, 2002 |
| PD-Rx Pharmaceuticals, Inc. | 2 | capsule | Generic drugs (ANDA) | July 11, 2025 |
| Proficient Rx LP | 2 | capsule | Generic drugs (ANDA) | January 30, 2002 |
| QPharma, Inc. | 2 | capsule | Generic drugs (ANDA) | July 11, 2025 |
| ScieGen Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 20, 2019 |
| Strides Pharma Science Limited | 2 | tablet | Generic drugs (ANDA) | August 12, 2024 |
| Teva Pharmaceuticals USA, Inc. | 2 | capsule | Generic drugs (ANDA) | January 29, 2002 |
| Torrent Pharmaceuticals Limited | 2 | tablet | Generic drugs (ANDA) | October 21, 2016 |
| Advanced Rx of Tennessee, LLC | 1 | capsule | Generic drugs (ANDA) | April 11, 2023 |
| American Health Packaging | 1 | solution | Generic drugs (ANDA) | December 4, 2024 |
| American Health Packaging | 1 | capsule | Generic drugs (ANDA) | July 14, 2026 |
| Aurobindo Pharma Limited | 1 | solution | Generic drugs (ANDA) | March 19, 2009 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | November 16, 2017 |
| Chartwell Governmental & Specialty RX, LLC. | 1 | liquid | Generic drugs (ANDA) | May 14, 2004 |
| Chartwell RX, LLC | 1 | liquid | Generic drugs (ANDA) | May 14, 2004 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 8, 2018 |
| Dr. Reddy's Laboratories Limited | 1 | tablet, film coated | Generic drugs (ANDA) | September 30, 2016 |
| PD-Rx Pharmaceuticals, Inc. | 1 | capsule | Generic drugs (ANDA) | January 29, 2016 |
| Par Health USA, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | November 16, 2017 |
| Preferred Pharmaceuticals Inc. | 1 | capsule | Generic drugs (ANDA) | March 28, 2024 |
| Proficient Rx LP | 1 | capsule | Generic drugs (ANDA) | January 29, 2002 |
| Saptalis Pharmaceuticals, LLC. | 1 | solution | Generic drugs (ANDA) | June 20, 2025 |
| Teva Pharmaceuticals USA, Inc. | 1 | capsule | Generic drugs (ANDA) | January 30, 2002 |
| Unit Dose Solutions, Inc. | 1 | capsule | Generic drugs (ANDA) | June 22, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 62 | 65.3% |
| Tablet, film coated | 23 | 24.2% |
| Tablet | 5 | 5.3% |
| Solution | 3 | 3.2% |
| Liquid | 2 | 2.1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 95 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Serotonin Reuptake Inhibitor | 95 |
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.