Data / Drug companies / Fesoterodine fumarate
Fesoterodine fumarate: 12 companies and 24 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Fesoterodine fumarate is listed in the FDA National Drug Code Directory by 12 companies, with 24 products in commercial distribution. 22 of the products (91.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, extended release; tablet, extended release, and the newest product started marketing on May 1, 2024.
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- Companies listing it
- 12
- Products
- 24
- Generic (ANDA) products
- 22 (91.7%)
- Application numbers
- 8
- Routes
- Oral
- Brand names
- Toviaz
- openFDA record search
- api.fda.gov
Companies that list fesoterodine fumarate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Alembic Pharmaceuticals Inc. | 2 | tablet, extended release | Generic drugs (ANDA) | January 6, 2023 |
| Alembic Pharmaceuticals Limited | 2 | tablet, extended release | Generic drugs (ANDA) | January 6, 2023 |
| Amneal Pharmaceuticals LLC | 2 | tablet, extended release | Generic drugs (ANDA) | January 6, 2023 |
| Ascend Laboratories, LLC | 2 | tablet, extended release | Generic drugs (ANDA) | June 9, 2022 |
| Aurobindo Pharma Limited | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | June 17, 2022 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | January 9, 2024 |
| Dr. Reddy's Laboratories Inc. | 2 | tablet, extended release | Generic drugs (ANDA) | June 10, 2022 |
| Golden State Medical Supply, Inc. | 2 | tablet, extended release | Generic drugs (ANDA) | August 13, 2019 |
| NorthStar RxLLC | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | May 1, 2024 |
| Pfizer Laboratories Div Pfizer Inc | 2 | tablet, film coated, extended release | New drug applications (NDA) | October 31, 2008 |
| Zydus Lifesciences Limited | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | December 7, 2017 |
| Zydus Pharmaceuticals USA Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | December 7, 2017 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 12 | 50% |
| Tablet, extended release | 12 | 50% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 22 | 91.7% |
| New drug applications (NDA) | 2 | 8.3% |
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.