Skip to the page

Data / Drug companies / Ticagrelor

Ticagrelor: 32 companies and 57 products in the FDA NDC directory

Ticagrelor is listed in the FDA National Drug Code Directory by 32 companies, with 57 products in commercial distribution. 53 of the products (93.0%) 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 November 1, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
32
Products
57
Generic (ANDA) products
53 (93.0%)
Application numbers
20
Routes
Oral
Brand names
Brilinta
openFDA record search
api.fda.gov

Companies that list ticagrelor

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Aphena Pharma Solutions - Tennessee, LLC3tablet; tablet, film coatedGeneric drugs (ANDA)May 7, 2025
AiPing Pharmaceutical, Inc.2tabletGeneric drugs (ANDA)June 10, 2026
Alembic Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)October 28, 2025
Alembic Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)October 28, 2025
American Health Packaging2tabletGeneric drugs (ANDA)February 18, 2026
Apotex Corp.2tabletGeneric drugs (ANDA)October 31, 2025
Ascend Laboratories, LLC2tablet; tablet, film coatedGeneric drugs (ANDA)October 28, 2025
AstraZeneca Pharmaceuticals LP2tabletNew drug applications (NDA)September 4, 2015
AvKARE2tabletGeneric drugs (ANDA)October 9, 2025
Bionpharma Inc.2tabletGeneric drugs (ANDA)October 28, 2025
Changzhou Pharmaceutical Factory2tabletGeneric drugs (ANDA)October 28, 2025
Cipla USA Inc.2tablet, film coatedGeneric drugs (ANDA)October 29, 2025
Dr. Reddy's Laboratories Inc.2tabletGeneric drugs (ANDA)October 28, 2025
Exelan Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)October 29, 2025
Laurus Labs Limited2tabletGeneric drugs (ANDA)August 20, 2026
Lifestar Pharma LLC2tablet, film coatedGeneric drugs (ANDA)February 6, 2026
Macleods Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)October 28, 2025
Mylan Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)September 25, 2025
NorthStar RxLLC2tablet, film coatedGeneric drugs (ANDA)August 10, 2026
Novadoz Pharmaceuticals LLC2tabletGeneric drugs (ANDA)July 19, 2025
Oryza Pharmaceuticals Inc.2tabletGeneric drugs (ANDA)December 1, 2025
Radha Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)October 9, 2025
ScieGen Pharmaceuticals, Inc.2tabletGeneric drugs (ANDA)October 9, 2025
Teva Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)May 1, 2025
Aphena Pharma Solutions - Tennessee, LLC1tabletGeneric drugs (ANDA)April 24, 2025
AvPAK1tabletGeneric drugs (ANDA)October 29, 2025
Cardinal Health 107, LLC1tabletNew drug applications (NDA)August 5, 2011
Golden State Medical Supply, Inc.1tabletGeneric drugs (ANDA)May 1, 2025
Hisun Pharmaceuticals USA, Inc.1tablet, film coatedGeneric drugs (ANDA)May 1, 2025
Micro Labs Limited1tablet, film coatedGeneric drugs (ANDA)November 1, 2026
Redpharm Drug1tablet, film coatedGeneric drugs (ANDA)May 1, 2025
Solco Healthcare US, LLC1tablet, film coatedGeneric drugs (ANDA)April 1, 2025

Dosage forms

Dosage formProductsShare
Tablet3357.9%
Tablet, film coated2442.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)5393%
New drug applications (NDA)47%

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.