Data / Drug companies / Darifenacin
Darifenacin: 7 companies and 14 products in the FDA NDC directory
Darifenacin is listed in the FDA National Drug Code Directory by 7 companies, with 14 products in commercial distribution. 14 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, extended release; tablet, film coated, extended release, and the newest product started marketing on December 12, 2017.
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- Companies listing it
- 7
- Products
- 14
- Generic (ANDA) products
- 14 (100.0%)
- Application numbers
- 4
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list darifenacin
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) | December 12, 2017 |
| Alembic Pharmaceuticals Limited | 2 | tablet, extended release | Generic drugs (ANDA) | December 12, 2017 |
| Aurobindo Pharma Limited | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | September 19, 2016 |
| Bryant Ranch Prepack | 2 | tablet, extended release | Generic drugs (ANDA) | November 18, 2016 |
| Macleods Pharmaceuticals Limited | 2 | tablet, extended release | Generic drugs (ANDA) | July 29, 2017 |
| Rising Pharma Holdings, Inc. | 2 | tablet, film coated, extended release | Generic drugs (ANDA) | September 19, 2016 |
| Torrent Pharmaceuticals Limited | 2 | tablet, extended release | Generic drugs (ANDA) | November 18, 2016 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, extended release | 10 | 71.4% |
| Tablet, film coated, extended release | 4 | 28.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 14 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cholinergic Muscarinic Antagonist | 14 |
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.