Data / Drug companies / Imatinib mesylate
Imatinib mesylate: 17 companies and 36 products in the FDA NDC directory
Imatinib mesylate is listed in the FDA National Drug Code Directory by 17 companies, with 36 products in commercial distribution. 33 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; tablet, and the newest product started marketing on July 3, 2026.
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- Companies listing it
- 17
- Products
- 36
- Generic (ANDA) products
- 33 (91.7%)
- Application numbers
- 9
- Routes
- Oral
- Brand names
- Gleevec
- openFDA record search
- api.fda.gov
Companies that list imatinib mesylate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| BluePoint Laboratories | 4 | tablet, film coated | Generic drugs (ANDA) | December 6, 2024 |
| Novartis Pharmaceuticals Corporation | 3 | tablet | New drug applications (NDA) | December 23, 2014 |
| Apotex Corp. | 2 | tablet, film coated | Generic drugs (ANDA) | August 5, 2016 |
| Archis Pharma LLC | 2 | tablet | Generic drugs (ANDA) | September 1, 2022 |
| Armas Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 15, 2019 |
| Ascend Laboratories, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | February 1, 2019 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | July 23, 2020 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 14, 2025 |
| Chartwell RX, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | January 17, 2019 |
| CivicaScript LLC | 2 | tablet, film coated | Generic drugs (ANDA) | July 3, 2026 |
| Major Pharmaceuticals | 2 | tablet, film coated | Generic drugs (ANDA) | August 5, 2016 |
| Qilu Pharmaceutical Co., Ltd. | 2 | tablet | Generic drugs (ANDA) | June 21, 2022 |
| Quallent Pharmaceuticals Health LLC | 2 | tablet, film coated | Generic drugs (ANDA) | September 1, 2023 |
| Sun Pharmaceutical Industries, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | February 1, 2016 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | August 4, 2016 |
| Upsher-Smith Laboratories, LLC | 2 | tablet | Generic drugs (ANDA) | May 17, 2024 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | February 19, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 27 | 75% |
| Tablet | 9 | 25% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 33 | 91.7% |
| New drug applications (NDA) | 3 | 8.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Kinase Inhibitor | 36 |
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.