Data / Drug companies / Sumatriptan
Sumatriptan: 28 companies and 53 products in the FDA NDC directory
Sumatriptan is listed in the FDA National Drug Code Directory by 28 companies, with 53 products in commercial distribution. 43 of the products (81.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; injection, solution; spray, and the newest product started marketing on June 1, 2026.
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- Companies listing it
- 28
- Products
- 53
- Generic (ANDA) products
- 43 (81.1%)
- Application numbers
- 21
- Routes
- Oral, Subcutaneous, Nasal
- Brand names
- Imitrex, Tosymra, Tosymra
- openFDA record search
- api.fda.gov
Companies that list sumatriptan
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| GlaxoSmithKline LLC | 6 | tablet, film coated; injection | New drug applications (NDA) | April 6, 2006 |
| A-S Medication Solutions | 4 | tablet, film coated; injection | Generic drugs (ANDA) | May 5, 2025 |
| Advanced Rx of Tennessee, LLC | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | December 30, 2024 |
| Onesource Specialty Pharma Limited | 4 | injection, solution | Generic drugs (ANDA) | February 2, 2026 |
| Bionpharma Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | February 18, 2022 |
| Rising Pharma Holdings, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | May 5, 2025 |
| Bryant Ranch Prepack | 2 | spray | Generic drugs (ANDA) | October 4, 2020 |
| Eugia US LLC | 2 | injection, solution | Generic drugs (ANDA) | April 23, 2013 |
| Lannett Company, Inc. | 2 | spray | Generic drugs (ANDA) | February 19, 2016 |
| Padagis Israel Pharmaceuticals Ltd | 2 | spray | Generic drugs (ANDA) | October 4, 2020 |
| Prasco Laboratories | 2 | spray | Authorized generics (NDA) | July 1, 2020 |
| Preferred Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 29, 2024 |
| Proficient Rx LP | 2 | tablet | Generic drugs (ANDA) | August 13, 2009 |
| Armas Pharmaceuticals Inc. | 1 | injection, solution | Generic drugs (ANDA) | June 1, 2026 |
| Baxter Healthcare Corporation | 1 | injection | Generic drugs (ANDA) | January 19, 2023 |
| Caplin Steriles Limited | 1 | injection, solution | Generic drugs (ANDA) | September 28, 2024 |
| Cipla USA Inc. | 1 | spray | Generic drugs (ANDA) | February 22, 2021 |
| Direct_Rx | 1 | tablet, film coated | Generic drugs (ANDA) | December 13, 2022 |
| Florida Pharmaceutical Products, LLC | 1 | spray | Generic drugs (ANDA) | May 15, 2021 |
| Golden State Medical Supply, Inc. | 1 | injection, solution | Generic drugs (ANDA) | June 10, 2010 |
| Hikma Pharmaceuticals USA Inc. | 1 | injection | Generic drugs (ANDA) | September 16, 2013 |
| NuCare Pharmaceuticals,Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | February 18, 2022 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | February 18, 2022 |
| Somerset Therapeutics, LLC | 1 | injection, solution | Generic drugs (ANDA) | October 25, 2021 |
| Sportpharm LLC | 1 | injection, solution | Generic drugs (ANDA) | April 23, 2013 |
| Strides Pharma Science Limited | 1 | injection, solution | Generic drugs (ANDA) | March 16, 2026 |
| Tonix Medicines, Inc. | 1 | spray | New drug applications (NDA) | July 1, 2023 |
| Upsher-Smith Laboratories, LLC | 1 | spray | New drug applications (NDA) | July 8, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 18 | 34% |
| Injection, solution | 13 | 24.5% |
| Spray | 12 | 22.6% |
| Injection | 6 | 11.3% |
| Tablet | 4 | 7.5% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 43 | 81.1% |
| New drug applications (NDA) | 8 | 15.1% |
| Authorized generics (NDA) | 2 | 3.8% |
Pharmacologic classes
| Class | Products |
|---|---|
| Serotonin-1b and Serotonin-1d Receptor Agonist | 53 |
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.