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Data / Drug companies / Anti-anginal

Anti-anginal drugs: 1 drug from 30 companies in the FDA NDC directory

Anti-anginal is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 53 products in this class from 30 companies, covering 1 drug by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on August 10, 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.

  • 30Companies
  • 53Products
  • 1Drugs by generic name

Drugs in the Anti-anginal class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Ranolazine5330

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A2A Integrated Pharmaceuticals2tablet, film coated, extended releaseGeneric drugs (ANDA)April 8, 2025
Ajanta Pharma USA Inc.2tablet, extended releaseGeneric drugs (ANDA)August 23, 2019
Aphena Pharma Solutions - Tennessee, LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)June 30, 2025
Ascend Laboratories, LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)December 2, 2020
Aurobindo Pharma Limited2tablet, film coated, extended releaseGeneric drugs (ANDA)December 23, 2022
AvKARE2tablet, film coated, extended releaseGeneric drugs (ANDA)October 27, 2020
AvPAK2tablet, film coated, extended releaseGeneric drugs (ANDA)September 20, 2022
Camber Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)May 5, 2022
Glenmark Pharmaceuticals Inc., USA2tablet, film coated, extended releaseGeneric drugs (ANDA)July 5, 2019
I3 Pharmaceuticals, LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)June 15, 2022
Lifestar Pharma LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)April 1, 2020
Lupin Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)February 27, 2019
Proficient Rx LP2tablet, film coated, extended releaseGeneric drugs (ANDA)August 24, 2021
Radha Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)June 30, 2025
ScieGen Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)June 4, 2019
SunGen Pharma LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)April 1, 2020
Torrent Pharmaceuticals Limited2tablet, film coated, extended releaseGeneric drugs (ANDA)May 11, 2026
Umedica Laboratories USA Inc.2tablet, extended releaseGeneric drugs (ANDA)August 10, 2026
Unichem Pharmaceuticals (USA), Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)March 16, 2023
Viona Pharmaceuticals Inc2tablet, extended releaseGeneric drugs (ANDA)September 10, 2019
Westminster Pharmaceuticals, LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)August 24, 2021
Zameer Pharmaceuticals LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)April 22, 2026
Zydus Lifesciences Limited2tablet, extended releaseGeneric drugs (ANDA)September 10, 2019
American Health Packaging1tablet, extended releaseGeneric drugs (ANDA)August 19, 2020
Bryant Ranch Prepack1tablet, film coated, extended releaseGeneric drugs (ANDA)June 15, 2022
Bryant Ranch Prepack1tablet, extended releaseGeneric drugs (ANDA)September 10, 2019
Major Pharmaceuticals1tablet, film coated, extended releaseGeneric drugs (ANDA)January 17, 2025
NCS HealthCare of Ky, LLC DBA Vangard Labs1tablet, extended releaseGeneric drugs (ANDA)September 10, 2019
Proficient Rx LP1tablet, film coated, extended releaseGeneric drugs (ANDA)August 24, 2021
Sun Pharmaceutical Industries, Inc.1granuleNew drug applications (NDA)February 28, 2022

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release4177.4%
Tablet, extended release1120.8%
Granule11.9%

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.