Data / Drug companies / Glinide
Glinide drugs: 2 drugs from 17 companies in the FDA NDC directory
Glinide is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 38 products in this class from 17 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on April 8, 2025.
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- 17Companies
- 38Products
- 2Drugs by generic name
Drugs in the Glinide class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Repaglinide | 20 | 9 |
| Nateglinide | 18 | 9 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| American Health Packaging | 3 | tablet | Generic drugs (ANDA) | January 12, 2023 |
| Aurobindo Pharma Limited | 3 | tablet | Generic drugs (ANDA) | January 22, 2014 |
| Chartwell RX, LLC | 3 | tablet | Generic drugs (ANDA) | January 22, 2014 |
| Macleods Pharmaceuticals Limited | 3 | tablet | Generic drugs (ANDA) | March 22, 2023 |
| NorthStar RxLLC | 3 | tablet | Generic drugs (ANDA) | April 8, 2025 |
| Rising Pharma Holdings, Inc. | 3 | tablet | Generic drugs (ANDA) | January 22, 2014 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | March 22, 2023 |
| Cadila Pharmaceuticals Limited | 2 | tablet, coated | Generic drugs (ANDA) | February 10, 2014 |
| Dr. Reddy's Laboratories Limited | 2 | tablet | Generic drugs (ANDA) | September 9, 2009 |
| Golden State Medical Supply, Inc. | 2 | tablet | Generic drugs (ANDA) | September 9, 2009 |
| Modavar Pharmaceuticals LLC | 2 | tablet, coated | Generic drugs (ANDA) | August 19, 2021 |
| Rising Pharma Holdings, Inc. | 2 | tablet | Generic drugs (ANDA) | December 16, 2020 |
| Strides Pharma Science Limited | 2 | tablet | Generic drugs (ANDA) | May 9, 2022 |
| Zydus Lifesciences Limited | 2 | tablet, film coated | Generic drugs (ANDA) | October 27, 2016 |
| Zydus Pharmaceuticals USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | October 27, 2016 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | January 22, 2014 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | January 22, 2014 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 30 | 78.9% |
| Tablet, film coated | 4 | 10.5% |
| Tablet, coated | 4 | 10.5% |
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.