Data / Drug companies / Eszopiclone
Eszopiclone: 29 companies and 92 products in the FDA NDC directory
Eszopiclone is listed in the FDA National Drug Code Directory by 29 companies, with 92 products in commercial distribution. 89 of the products (96.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, coated, and the newest product started marketing on July 24, 2025.
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- Companies listing it
- 29
- Products
- 92
- Generic (ANDA) products
- 89 (96.7%)
- Application numbers
- 11
- Controlled substance schedule
- Schedule IV
- Routes
- Oral, Oropharyngeal
- Brand names
- Lunesta
- openFDA record search
- api.fda.gov
Companies that list eszopiclone
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Advanced Rx of Tennessee, LLC | 10 | tablet, film coated; tablet, coated | Generic drugs (ANDA) | June 24, 2024 |
| Bryant Ranch Prepack | 8 | tablet, film coated | Generic drugs (ANDA) | September 15, 2016 |
| Asclemed USA, Inc. | 6 | tablet, film coated | Generic drugs (ANDA) | January 31, 2015 |
| Preferred Pharmaceuticals Inc. | 5 | tablet, film coated | Generic drugs (ANDA) | February 10, 2025 |
| Proficient Rx LP | 5 | tablet, film coated | Generic drugs (ANDA) | September 15, 2016 |
| A-S Medication Solutions | 4 | tablet, film coated | Generic drugs (ANDA) | September 15, 2016 |
| Remedyrepack Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | July 24, 2025 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | September 15, 2016 |
| Bionpharma Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | June 1, 2022 |
| Camber Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | January 4, 2024 |
| Dr. Reddy's Laboratories Limited | 3 | tablet, coated | Generic drugs (ANDA) | April 15, 2014 |
| Glenmark Pharmaceuticals Inc., USA | 3 | tablet, film coated | Generic drugs (ANDA) | April 15, 2014 |
| Golden State Medical Supply, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 26, 2013 |
| Lupin Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | April 15, 2014 |
| Macleods Pharmaceuticals Limited | 3 | tablet, film coated | Generic drugs (ANDA) | January 31, 2015 |
| Mylan Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 26, 2013 |
| Proficient Rx LP | 3 | tablet, film coated | Generic drugs (ANDA) | April 25, 2014 |
| Sun Pharmaceutical Industries, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | April 15, 2014 |
| Waylis Therapeutics LLC | 3 | tablet, coated | New drug applications (NDA) | August 15, 2023 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 25, 2014 |
| Proficient Rx LP | 2 | tablet, film coated | Generic drugs (ANDA) | January 4, 2024 |
| Quality Care Products, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | May 4, 2018 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 14, 2014 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | April 14, 2014 |
| Direct RX | 1 | tablet, film coated | Generic drugs (ANDA) | February 13, 2017 |
| Direct_Rx | 1 | tablet, film coated | Generic drugs (ANDA) | June 10, 2020 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 15, 2014 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | September 15, 2016 |
| St. Mary's Medical Park Pharmacy | 1 | tablet, film coated | Generic drugs (ANDA) | June 7, 2021 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 84 | 91.3% |
| Tablet, coated | 8 | 8.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 89 | 96.7% |
| New drug applications (NDA) | 3 | 3.3% |
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.