Data / Drug companies / Riluzole
Riluzole: 7 companies and 10 products in the FDA NDC directory
Riluzole is listed in the FDA National Drug Code Directory by 7 companies, with 10 products in commercial distribution. 5 of the products (50.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are liquid; tablet, film coated; suspension, and the newest product started marketing on June 10, 2024.
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- Companies listing it
- 7
- Products
- 10
- Generic (ANDA) products
- 5 (50.0%)
- Application numbers
- 5
- Routes
- Oral
- Brand names
- Teglutik, Tiglutik
- openFDA record search
- api.fda.gov
Companies that list riluzole
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Edw Pharma, Inc | 4 | liquid | Unapproved drugs for a shortage | June 10, 2024 |
| Ascend Laboratories, LLC | 1 | tablet | Generic drugs (ANDA) | March 31, 2016 |
| AvKARE | 1 | tablet, film coated | Generic drugs (ANDA) | October 7, 2020 |
| Glenmark Pharmaceuticals Inc., USA | 1 | tablet, film coated | Generic drugs (ANDA) | June 18, 2013 |
| Italfarmaco SpA | 1 | suspension | New drug applications (NDA) | September 21, 2018 |
| Quinn Pharmaceuticals | 1 | tablet, film coated | Generic drugs (ANDA) | January 1, 2020 |
| Sun Pharmaceutical Industries, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | June 18, 2013 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 4 | 40% |
| Tablet, film coated | 4 | 40% |
| Suspension | 1 | 10% |
| Tablet | 1 | 10% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 5 | 50% |
| Unapproved drugs for a shortage | 3 | 30% |
| New drug applications (NDA) | 2 | 20% |
Pharmacologic classes
| Class | Products |
|---|---|
| Benzothiazole | 10 |
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.