Data / Drug companies / Gemfibrozil
Gemfibrozil: 29 companies and 43 products in the FDA NDC directory
Gemfibrozil is listed in the FDA National Drug Code Directory by 29 companies, with 43 products in commercial distribution. 43 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated, and the newest product started marketing on September 24, 2026.
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- Companies listing it
- 29
- Products
- 43
- Generic (ANDA) products
- 43 (100.0%)
- Application numbers
- 8
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list gemfibrozil
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 6 | tablet; tablet, film coated | Generic drugs (ANDA) | January 20, 2021 |
| Aphena Pharma Solutions - Tennessee, LLC | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | January 20, 2021 |
| Bryant Ranch Prepack | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | January 20, 2021 |
| Remedyrepack Inc. | 3 | tablet; tablet, film coated | Generic drugs (ANDA) | September 24, 2026 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet | Generic drugs (ANDA) | January 20, 2021 |
| American Health Packaging | 1 | tablet | Generic drugs (ANDA) | July 7, 2016 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | September 16, 2015 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | July 10, 2014 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | January 20, 2021 |
| Cadila Pharmaceuticals Limited | 1 | tablet | Generic drugs (ANDA) | June 17, 2016 |
| Camber Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | January 20, 2021 |
| Chartwell RX, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 27, 1993 |
| Cipla USA Inc. | 1 | tablet | Generic drugs (ANDA) | October 13, 2016 |
| Coupler LLC | 1 | tablet | Generic drugs (ANDA) | April 29, 2026 |
| Exelan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 20, 2006 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 1 | tablet, film coated | Generic drugs (ANDA) | September 16, 2015 |
| NorthStar Rx LLC | 1 | tablet | Generic drugs (ANDA) | December 20, 2010 |
| NorthStar RxLLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 16, 2015 |
| Northwind Health Company, LLC | 1 | tablet | Generic drugs (ANDA) | August 14, 2017 |
| NuCare Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | July 8, 2016 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | October 13, 2016 |
| Preferred Pharmaceuticals Inc. | 1 | tablet | Generic drugs (ANDA) | July 20, 2021 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | January 20, 2021 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | July 8, 2016 |
| Rising Pharma Holdings, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | September 16, 2015 |
| Viona Pharmaceuticals Inc | 1 | tablet | Generic drugs (ANDA) | February 21, 2020 |
| XLCare Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | January 20, 2021 |
| Zydus Lifesciences Limited | 1 | tablet | Generic drugs (ANDA) | February 21, 2020 |
| Zydus Pharmaceuticals USA Inc. | 1 | tablet | Generic drugs (ANDA) | January 15, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 31 | 72.1% |
| Tablet, film coated | 12 | 27.9% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 43 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Peroxisome Proliferator Receptor alpha Agonist | 43 |
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.