Data / Drug companies / Armodafinil
Armodafinil: 12 companies and 37 products in the FDA NDC directory
Armodafinil is listed in the FDA National Drug Code Directory by 12 companies, with 37 products in commercial distribution. 18 of the products (48.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on August 31, 2025.
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- Companies listing it
- 12
- Products
- 37
- Generic (ANDA) products
- 18 (48.6%)
- Application numbers
- 4
- Controlled substance schedule
- Schedule IV
- Routes
- Oral
- Brand names
- Nuvigil
- openFDA record search
- api.fda.gov
Companies that list armodafinil
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Apotex Corp. | 4 | tablet | New drug applications (NDA) | August 31, 2025 |
| Aurobindo Pharma Limited | 4 | tablet | Generic drugs (ANDA) | December 7, 2018 |
| Direct_Rx | 4 | tablet | Generic drugs (ANDA) | May 3, 2023 |
| Golden State Medical Supply, Inc. | 4 | tablet | New drug applications (NDA) | March 26, 2009 |
| Natco Pharma USA LLC | 4 | tablet | Generic drugs (ANDA) | March 23, 2023 |
| Sandoz Inc | 4 | tablet | Authorized generics (NDA) | December 1, 2016 |
| Bryant Ranch Prepack | 3 | tablet | Generic drugs (ANDA) | March 6, 2018 |
| Mylan Pharmaceuticals Inc. | 3 | tablet | Generic drugs (ANDA) | June 1, 2016 |
| Teva Pharmaceuticals USA, Inc. | 3 | tablet | Authorized generics (NDA) | November 29, 2016 |
| Preferred Pharmaceuticals Inc. | 2 | tablet | Generic drugs (ANDA) | March 8, 2021 |
| Cephalon, LLC | 1 | tablet | New drug applications (NDA) | May 26, 2009 |
| Quality Care Products, LLC | 1 | tablet | Authorized generics (NDA) | November 29, 2016 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 37 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 18 | 48.6% |
| Authorized generics (NDA) | 10 | 27% |
| New drug applications (NDA) | 9 | 24.3% |
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.