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Data / Drug companies / Esmolol hydrochloride

Esmolol hydrochloride: 12 companies and 28 products in the FDA NDC directory

Esmolol hydrochloride is listed in the FDA National Drug Code Directory by 12 companies, with 28 products in commercial distribution. 15 of the products (53.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection; injection, solution, and the newest product started marketing on July 29, 2025.

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Companies listing it
12
Products
28
Generic (ANDA) products
15 (53.6%)
Application numbers
7
Routes
Intravenous
Brand names
Brevibloc, Brevibloc
openFDA record search
api.fda.gov

Companies that list esmolol hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Baxter Healthcare Company8injectionNew drug applications (NDA)December 31, 1986
HF Acquisition Co LLC, DBA HealthFirst4injection, solution; injectionGeneric drugs (ANDA)December 22, 2019
Henry Schein, Inc.3injection, solution; injectionGeneric drugs (ANDA)June 10, 2025
Fresenius Kabi USA, LLC2injection, solutionGeneric drugs (ANDA)November 30, 2004
Medical Purchasing Solutions, LLC2injection; injection, solutionNew drug applications (NDA)July 23, 2015
Sagent Pharmaceuticals2injection, solutionGeneric drugs (ANDA)July 15, 2019
WG Critical Care, LLC2injectionNew drug applications (NDA)December 4, 2017
Eugia US LLC1injection, solutionGeneric drugs (ANDA)July 23, 2015
Gland Pharma Limited1injectionGeneric drugs (ANDA)August 19, 2019
Mylan Institutional LLC1injection, solutionGeneric drugs (ANDA)May 29, 2007
ProPharma Distribution1injection, solutionGeneric drugs (ANDA)July 23, 2015
Remedyrepack Inc.1injection, solutionGeneric drugs (ANDA)July 29, 2025

Dosage forms

Dosage formProductsShare
Injection1450%
Injection, solution1450%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1553.6%
New drug applications (NDA)1346.4%

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.