Data / Drug companies / Felbamate
Felbamate: 11 companies and 22 products in the FDA NDC directory
Felbamate is listed in the FDA National Drug Code Directory by 11 companies, with 22 products in commercial distribution. 20 of the products (90.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; suspension, and the newest product started marketing on August 10, 2022.
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- Companies listing it
- 11
- Products
- 22
- Generic (ANDA) products
- 20 (90.9%)
- Application numbers
- 8
- Routes
- Oral
- Brand names
- Felbatol
- openFDA record search
- api.fda.gov
Companies that list felbamate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Amneal Pharmaceuticals LLC | 3 | tablet; suspension | Generic drugs (ANDA) | December 16, 2011 |
| Sun Pharmaceutical Industries, Inc. | 3 | tablet; suspension | Generic drugs (ANDA) | June 16, 2017 |
| Amneal Pharmaceuticals of New York LLC | 2 | tablet | Generic drugs (ANDA) | August 10, 2022 |
| Ani Pharmaceuticals, Inc. | 2 | tablet | Generic drugs (ANDA) | September 4, 2018 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | September 4, 2018 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | September 4, 2018 |
| Viatris Specialty LLC | 2 | tablet | New drug applications (NDA) | July 29, 1993 |
| Viona Pharmaceuticals Inc | 2 | tablet | Generic drugs (ANDA) | March 3, 2020 |
| Zydus Lifesciences Limited | 2 | tablet | Generic drugs (ANDA) | August 15, 2017 |
| Ani Pharmaceuticals, Inc. | 1 | suspension | Generic drugs (ANDA) | July 15, 2022 |
| NorthStar Rx LLC | 1 | suspension | Generic drugs (ANDA) | April 10, 2018 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 18 | 81.8% |
| Suspension | 4 | 18.2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 20 | 90.9% |
| New drug applications (NDA) | 2 | 9.1% |
Pharmacologic classes
| Class | Products |
|---|---|
| Anti-epileptic Agent | 22 |
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.