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Data / Drug companies / beta3-Adrenergic Agonist

beta3-Adrenergic Agonist drugs: 2 drugs from 11 companies in the FDA NDC directory

beta3-Adrenergic Agonist is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 24 products in this class from 11 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 30, 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.

  • 11Companies
  • 24Products
  • 2Drugs by generic name

Drugs in the beta3-Adrenergic Agonist class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Mirabegron2310
Vibegron11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack4tablet, film coated, extended releaseGeneric drugs (ANDA)September 3, 2024
Astellas Pharma US, Inc.3tablet, film coated, extended release; granule, for suspension, extended releaseNew drug applications (NDA)March 25, 2021
Remedyrepack Inc.3tablet, extended release; tablet, film coated, extended releaseGeneric drugs (ANDA)May 22, 2026
Amneal Pharmaceuticals NY LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)April 19, 2026
AvKARE2tablet, film coated, extended releaseGeneric drugs (ANDA)October 30, 2026
Lupin Pharmaceuticals, Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)September 3, 2024
Qilu Pharmaceutical Co., Ltd.2tablet, film coated, extended releaseGeneric drugs (ANDA)June 30, 2025
Zydus Lifesciences Limited2tablet, extended releaseGeneric drugs (ANDA)January 23, 2024
Zydus Pharmaceuticals USA Inc.2tablet, extended releaseGeneric drugs (ANDA)January 23, 2024
Ascend Laboratories, LLC1for suspension, extended releaseGeneric drugs (ANDA)June 15, 2026
Sumitomo Pharma America, Inc.1tablet, film coatedNew drug applications (NDA)December 29, 2020

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release1562.5%
Tablet, extended release625%
Tablet, film coated14.2%
Granule, for suspension, extended release14.2%
For suspension, extended release14.2%

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.