Data / Drug companies / Abiraterone acetate
Abiraterone acetate: 22 companies and 36 products in the FDA NDC directory
Abiraterone acetate is listed in the FDA National Drug Code Directory by 22 companies, with 36 products in commercial distribution. 32 of the products (88.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated, and the newest product started marketing on May 4, 2026.
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- Companies listing it
- 22
- Products
- 36
- Generic (ANDA) products
- 32 (88.9%)
- Application numbers
- 12
- Routes
- Oral
- Brand names
- Abiraterone, Zytiga, Abirtega, Yonsa
- openFDA record search
- api.fda.gov
Companies that list abiraterone acetate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Novadoz Pharmaceuticals LLC | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | April 24, 2024 |
| Apotex Corp. | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | July 16, 2021 |
| BluePoint Laboratories | 2 | tablet | Generic drugs (ANDA) | October 16, 2025 |
| CivicaScript LLC | 2 | tablet | Generic drugs (ANDA) | November 23, 2018 |
| Dr. Reddy's Laboratories Inc. | 2 | tablet | Generic drugs (ANDA) | September 11, 2023 |
| Florida Pharmaceutical Products, LLC | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | April 10, 2023 |
| Glenmark Pharmaceuticals Inc., USA | 2 | tablet | Generic drugs (ANDA) | May 19, 2022 |
| Golden State Medical Supply, Inc. | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | December 14, 2020 |
| Janssen Biotech, Inc. | 2 | tablet, film coated; tablet | New drug applications (NDA) | April 17, 2017 |
| Mylan Pharmaceuticals Inc. | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | December 14, 2020 |
| NorthStar RxLLC | 2 | tablet | Generic drugs (ANDA) | May 19, 2022 |
| Novugen Pharma (USA) LLC | 2 | tablet, film coated | Generic drugs (ANDA) | January 5, 2022 |
| Quallent Pharmaceuticals Health LLC | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | October 7, 2019 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | May 4, 2026 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | December 14, 2020 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet | Generic drugs (ANDA) | March 17, 2025 |
| Hikma Pharmaceuticals USA Inc. | 1 | tablet | Generic drugs (ANDA) | November 23, 2018 |
| Major Pharmaceuticals | 1 | tablet | Generic drugs (ANDA) | November 23, 2018 |
| NorthStar Rx LLC | 1 | tablet | Generic drugs (ANDA) | May 19, 2020 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | November 23, 2018 |
| Rising Pharma Holdings, Inc. | 1 | tablet | Generic drugs (ANDA) | February 25, 2019 |
| Sun Pharmaceutical Industries, Inc. | 1 | tablet | New drug applications (NDA) | May 22, 2018 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 25 | 69.4% |
| Tablet, film coated | 11 | 30.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 32 | 88.9% |
| New drug applications (NDA) | 4 | 11.1% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cytochrome P450 17A1 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.