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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.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Novadoz Pharmaceuticals LLC3tablet, film coated; tabletGeneric drugs (ANDA)April 24, 2024
Apotex Corp.2tablet, film coated; tabletGeneric drugs (ANDA)July 16, 2021
BluePoint Laboratories2tabletGeneric drugs (ANDA)October 16, 2025
CivicaScript LLC2tabletGeneric drugs (ANDA)November 23, 2018
Dr. Reddy's Laboratories Inc.2tabletGeneric drugs (ANDA)September 11, 2023
Florida Pharmaceutical Products, LLC2tablet, film coated; tabletGeneric drugs (ANDA)April 10, 2023
Glenmark Pharmaceuticals Inc., USA2tabletGeneric drugs (ANDA)May 19, 2022
Golden State Medical Supply, Inc.2tablet, film coated; tabletGeneric drugs (ANDA)December 14, 2020
Janssen Biotech, Inc.2tablet, film coated; tabletNew drug applications (NDA)April 17, 2017
Mylan Pharmaceuticals Inc.2tablet, film coated; tabletGeneric drugs (ANDA)December 14, 2020
NorthStar RxLLC2tabletGeneric drugs (ANDA)May 19, 2022
Novugen Pharma (USA) LLC2tablet, film coatedGeneric drugs (ANDA)January 5, 2022
Quallent Pharmaceuticals Health LLC2tablet, film coated; tabletGeneric drugs (ANDA)October 7, 2019
AvPAK1tabletGeneric drugs (ANDA)May 4, 2026
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)December 14, 2020
Dr. Reddy's Laboratories Inc.1tabletGeneric drugs (ANDA)March 17, 2025
Hikma Pharmaceuticals USA Inc.1tabletGeneric drugs (ANDA)November 23, 2018
Major Pharmaceuticals1tabletGeneric drugs (ANDA)November 23, 2018
NorthStar Rx LLC1tabletGeneric drugs (ANDA)May 19, 2020
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)November 23, 2018
Rising Pharma Holdings, Inc.1tabletGeneric drugs (ANDA)February 25, 2019
Sun Pharmaceutical Industries, Inc.1tabletNew drug applications (NDA)May 22, 2018

Dosage forms

Dosage formProductsShare
Tablet2569.4%
Tablet, film coated1130.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3288.9%
New drug applications (NDA)411.1%

Pharmacologic classes

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.