Data / Drug companies / Capecitabine
Capecitabine: 19 companies and 34 products in the FDA NDC directory
Capecitabine is listed in the FDA National Drug Code Directory by 19 companies, with 34 products in commercial distribution. 33 of the products (97.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on June 26, 2025.
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- Companies listing it
- 19
- Products
- 34
- Generic (ANDA) products
- 33 (97.1%)
- Application numbers
- 12
- Routes
- Oral
- Brand names
- Xeloda
- openFDA record search
- api.fda.gov
Companies that list capecitabine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Accord Healthcare Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 9, 2015 |
| Armas Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 1, 2019 |
| Ascend Laboratories, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 25, 2017 |
| Aurobindo Pharma Limited | 2 | tablet | Generic drugs (ANDA) | April 17, 2018 |
| BluePoint Laboratories | 2 | tablet, film coated | Generic drugs (ANDA) | April 22, 2025 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 5, 2024 |
| Cipla USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | July 1, 2023 |
| CivicaScript LLC | 2 | tablet, film coated | Generic drugs (ANDA) | June 26, 2025 |
| Dr. Reddy's Laboratories Limited | 2 | tablet | Generic drugs (ANDA) | December 10, 2020 |
| Golden State Medical Supply, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | September 16, 2013 |
| Lifestar Pharma LLC | 2 | tablet, film coated | Generic drugs (ANDA) | September 1, 2020 |
| Novadoz Pharmaceuticals LLC | 2 | tablet, film coated | Generic drugs (ANDA) | July 21, 2018 |
| Sun Pharmaceutical Industries, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | September 1, 2019 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 7, 2014 |
| Teyro Labs Private Limited | 2 | tablet, film coated | Generic drugs (ANDA) | February 16, 2022 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | March 7, 2016 |
| H2-Pharma, LLC | 1 | tablet, film coated | New drug applications (NDA) | April 30, 1998 |
| NorthStar RxLLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 1, 2024 |
| Quallent Pharmaceuticals Health LLC | 1 | tablet | Generic drugs (ANDA) | July 21, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 29 | 85.3% |
| Tablet | 5 | 14.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 33 | 97.1% |
| New drug applications (NDA) | 1 | 2.9% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nucleoside Metabolic Inhibitor | 34 |
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.