Data / Drug companies / Escitalopram
Escitalopram: 34 companies and 102 products in the FDA NDC directory
Escitalopram is listed in the FDA National Drug Code Directory by 34 companies, with 102 products in commercial distribution. 98 of the products (96.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; solution, and the newest product started marketing on July 24, 2026.
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- Companies listing it
- 34
- Products
- 102
- Generic (ANDA) products
- 98 (96.1%)
- Application numbers
- 10
- Routes
- Oral
- Brand names
- Lexapro
- openFDA record search
- api.fda.gov
Companies that list escitalopram
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 11 | tablet, film coated | Generic drugs (ANDA) | June 10, 2023 |
| A-S Medication Solutions | 8 | tablet, film coated | Generic drugs (ANDA) | June 10, 2023 |
| Remedyrepack Inc. | 8 | tablet, film coated | Generic drugs (ANDA) | July 19, 2026 |
| Northwind Health Company, LLC | 7 | tablet, film coated | Generic drugs (ANDA) | September 8, 2022 |
| Direct_Rx | 4 | tablet, film coated; tablet | Generic drugs (ANDA) | March 30, 2023 |
| Preferred Pharmaceuticals Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | July 24, 2026 |
| Accord Healthcare Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 21, 2013 |
| Allergan, Inc. | 3 | tablet, film coated | New drug applications (NDA) | August 14, 2002 |
| Ascent Pharmaceuticals, Inc. | 3 | tablet | Generic drugs (ANDA) | July 15, 2025 |
| BluePoint Laboratories | 3 | tablet, film coated | Generic drugs (ANDA) | December 18, 2023 |
| Bryant Ranch Prepack | 3 | tablet, film coated | Generic drugs (ANDA) | September 11, 2012 |
| Cipla USA Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | June 16, 2016 |
| Coupler LLC | 3 | tablet, film coated | Generic drugs (ANDA) | April 28, 2026 |
| Exelan Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | October 1, 2012 |
| NuCare Pharmaceuticals,Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 21, 2013 |
| Proficient Rx LP | 3 | tablet, film coated | Generic drugs (ANDA) | March 21, 2013 |
| Rising Pharma Holdings, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | June 10, 2023 |
| Solco Healthcare US, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | February 1, 2016 |
| Torrent Pharmaceuticals Limited | 3 | tablet, film coated | Generic drugs (ANDA) | September 11, 2012 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | March 21, 2013 |
| Cardinal Health 107, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | October 15, 2014 |
| Legacy Pharmaceutical Packaging, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | June 16, 2016 |
| Major Pharmaceuticals | 2 | tablet, film coated | Generic drugs (ANDA) | October 15, 2014 |
| QPharma, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | February 1, 2016 |
| St. Mary's Medical Park Pharmacy | 2 | tablet, film coated | Generic drugs (ANDA) | June 12, 2024 |
| Advanced Rx of Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | April 11, 2023 |
| Almatica Pharma LLC | 1 | capsule | New drug applications (NDA) | October 6, 2025 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | March 20, 2025 |
| Amneal Pharmaceuticals LLC | 1 | solution | Generic drugs (ANDA) | September 3, 2011 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | October 1, 2012 |
| Macleods Pharmaceuticals Limited | 1 | solution | Generic drugs (ANDA) | March 31, 2016 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 19, 2013 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 21, 2013 |
| Redpharm Drug | 1 | tablet, film coated | Generic drugs (ANDA) | March 15, 2012 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 95 | 93.1% |
| Tablet | 4 | 3.9% |
| Solution | 2 | 2% |
| Capsule | 1 | 1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 98 | 96.1% |
| New drug applications (NDA) | 4 | 3.9% |
Pharmacologic classes
| Class | Products |
|---|---|
| Serotonin Reuptake Inhibitor | 102 |
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.