Data / Drug companies / Nateglinide
Nateglinide: 9 companies and 18 products in the FDA NDC directory
Nateglinide is listed in the FDA National Drug Code Directory by 9 companies, with 18 products in commercial distribution. 18 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; tablet, coated, and the newest product started marketing on January 12, 2023.
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- Companies listing it
- 9
- Products
- 18
- Generic (ANDA) products
- 18 (100.0%)
- Application numbers
- 5
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list nateglinide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| American Health Packaging | 2 | tablet | Generic drugs (ANDA) | January 12, 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 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 10 | 55.6% |
| Tablet, film coated | 4 | 22.2% |
| Tablet, coated | 4 | 22.2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 18 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Glinide | 18 |
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.