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Data / Drug companies / Atenolol

Atenolol: 36 companies and 129 products in the FDA NDC directory

Atenolol is listed in the FDA National Drug Code Directory by 36 companies, with 129 products in commercial distribution. 126 of the products (97.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on August 25, 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
36
Products
129
Generic (ANDA) products
126 (97.7%)
Application numbers
9
Routes
Oral
Brand names
Tenormin
openFDA record search
api.fda.gov

Companies that list atenolol

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions14tabletGeneric drugs (ANDA)November 21, 2019
Bryant Ranch Prepack10tabletGeneric drugs (ANDA)November 21, 2019
NuCare Pharmaceuticals,Inc.9tabletGeneric drugs (ANDA)November 21, 2019
Preferred Pharmaceuticals Inc.7tabletGeneric drugs (ANDA)April 22, 2026
Northwind Health Company, LLC6tabletGeneric drugs (ANDA)December 28, 2022
Direct_Rx4tabletGeneric drugs (ANDA)November 22, 2022
Remedyrepack Inc.4tabletGeneric drugs (ANDA)February 12, 2025
St. Mary's Medical Park Pharmacy4tabletGeneric drugs (ANDA)August 25, 2026
Aphena Pharma Solutions - Tennessee, LLC3tabletGeneric drugs (ANDA)November 16, 2004
Asclemed USA Inc.3tabletGeneric drugs (ANDA)November 21, 2019
Aurobindo Pharma Limited3tabletGeneric drugs (ANDA)October 31, 2007
Bryant Ranch Prepack3tabletGeneric drugs (ANDA)December 19, 2022
Cardinal Health 107, LLC3tabletGeneric drugs (ANDA)July 20, 2026
Coupler LLC3tabletGeneric drugs (ANDA)May 6, 2026
Golden State Medical Supply, Inc.3tabletGeneric drugs (ANDA)April 26, 1999
Ipca Laboratories Limited3tabletGeneric drugs (ANDA)December 4, 2007
Mylan Institutional Inc.3tabletGeneric drugs (ANDA)June 16, 1999
Mylan Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)June 17, 1999
PD-Rx Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)October 8, 2005
Proficient Rx LP3tabletGeneric drugs (ANDA)June 10, 2010
QPharma, Inc.3tabletGeneric drugs (ANDA)June 10, 2010
Rising Pharma Holdings, Inc.3tabletGeneric drugs (ANDA)June 10, 2010
Safecor Health, LLC3tabletGeneric drugs (ANDA)February 3, 2026
Teva Pharmaceuticals USA, Inc.3tabletGeneric drugs (ANDA)November 16, 2004
Unichem Pharmaceuticals (USA), Inc.3tabletGeneric drugs (ANDA)November 21, 2019
Upsher-Smith Laboratories, LLC3tabletNew drug applications (NDA)August 1, 2024
Zydus Lifesciences Limited3tabletGeneric drugs (ANDA)October 8, 2005
Zydus Pharmaceuticals USA Inc.3tabletGeneric drugs (ANDA)October 8, 2005
Aphena Pharma Solutions - Tennessee, LLC2tabletGeneric drugs (ANDA)February 20, 2014
NCS HealthCare of Ky, LLC DBA Vangard Labs2tabletGeneric drugs (ANDA)June 10, 2010
Proficient Rx LP2tabletGeneric drugs (ANDA)November 16, 2004
American Health Packaging1tabletGeneric drugs (ANDA)October 25, 2021
Major Pharmaceuticals1tabletGeneric drugs (ANDA)October 31, 2007
NuCare Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)October 8, 2005
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)October 8, 2005
Quality Care Products, LLC1tabletGeneric drugs (ANDA)January 25, 2024

Dosage forms

Dosage formProductsShare
Tablet129100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)12697.7%
New drug applications (NDA)32.3%

Pharmacologic classes

ClassProducts
beta-Adrenergic Blocker129

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.