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Data / Drug companies / beta Lactamase Inhibitor

beta Lactamase Inhibitor drugs: 17 drugs from 63 companies in the FDA NDC directory

beta Lactamase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 335 products in this class from 63 companies, covering 17 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on September 21, 2026.

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  • 63Companies
  • 335Products
  • 17Drugs by generic name

Drugs in the beta Lactamase Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Amoxicillin and clavulanate potassium20335
Piperacillin and tazobactam4713
Ampicillin sodium and sulbactam sodium247
Piperacillin sodium and tazobactam sodium215
Ampicillin and sulbactam134
Piperacillin sodium,tazobactam sodium92
Ampicillin sodium, sulbactam sodium42
Piperacillin and tazobactam and sodium chloride31
Tazobactam sodium and piperacillin sodium31
Amoxicillin/clav pot11
Amoxicillin/clav pot oral susp11
Aztreonam and avibactam11
Ceftazidime, avibactam11
Ceftolozane and tazobactam11
Imipenem anhydrous, cilastatin, and relebactam anhydrous11
Meropenem-vaborbactam11
Piperacillin sodium, tazobactam sodium11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
NuCare Pharmaceuticals,Inc.31tablet, film coated; powder, for suspensionGeneric drugs (ANDA)September 19, 2022
A-S Medication Solutions17powder, for suspension; tablet, film coatedGeneric drugs (ANDA)November 21, 2022
Eugia US LLC16injection, powder, for solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)October 12, 2023
Fresenius Kabi USA, LLC15injection, powder, for solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 18, 2018
Preferred Pharmaceuticals Inc.13tablet, film coated; powder, for suspensionGeneric drugs (ANDA)July 31, 2026
Sandoz Inc12injection, powder, lyophilized, for solution; tablet, film coatedGeneric drugs (ANDA)October 25, 2021
Remedyrepack Inc.10tablet, film coated; tabletGeneric drugs (ANDA)September 21, 2026
Asclemed USA, Inc.9tablet, film coated; powder, for suspensionGeneric drugs (ANDA)May 1, 2020
Proficient Rx LP9tablet, film coated; powder, for suspensionGeneric drugs (ANDA)January 20, 2012
PD-Rx Pharmaceuticals, Inc.8tablet, film coated; tabletGeneric drugs (ANDA)August 23, 2016
Sportpharm LLC8tablet, film coated; tablet, multilayer, extended releaseGeneric drugs (ANDA)August 12, 2019
WG Critical Care, LLC8injection, powder, for solutionGeneric drugs (ANDA)November 30, 2021
Avenacy, LLC7injection, powder, for solutionGeneric drugs (ANDA)September 1, 2025
Bryant Ranch Prepack7tablet, film coatedGeneric drugs (ANDA)March 1, 2017
Chartwell RX, LLC7powder, for suspension; tabletGeneric drugs (ANDA)March 22, 2005
Fresenius Kabi USA, LLC7injection, powder, lyophilized, for solution; injection, powder, for solutionGeneric drugs (ANDA)March 20, 2023
Proficient Rx LP7tablet, film coated; powder, for suspensionGeneric drugs (ANDA)May 1, 2020
Aurobindo Pharma Limited6tablet, film coated; powder, for suspensionGeneric drugs (ANDA)January 20, 2012
Meitheal Pharmaceuticals Inc.6injection, powder, for solutionGeneric drugs (ANDA)November 27, 2006
NorthStar Rx LLC6tablet, film coated; powder, for suspensionGeneric drugs (ANDA)January 20, 2012
Onesource Specialty Pharma Limited6injection, powder, for solutionGeneric drugs (ANDA)May 1, 2025
USAntibiotics, LLC6for suspension; tablet, coatedAuthorized generics (NDA)December 15, 2025
Armas Pharmaceuticals Inc.5injection, powder, for solutionGeneric drugs (ANDA)May 1, 2025
Bryant Ranch Prepack5tablet, film coatedGeneric drugs (ANDA)March 1, 2017
Civica, Inc.5injection, powder, for solutionGeneric drugs (ANDA)September 8, 2025
Devatis, Inc.5powder, for suspension; tablet, film coatedGeneric drugs (ANDA)November 1, 2024
Provepharm Inc.5injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 11, 2023
Teva Pharmaceuticals USA, Inc.5powder, for suspension; tablet, film coatedGeneric drugs (ANDA)January 13, 2005
Apotex Corp.4injection, powder, for solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 26, 2023
Hikma Pharmaceuticals USA Inc.4powder, for suspension; tabletGeneric drugs (ANDA)August 23, 2016
Hospira, Inc.4injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 14, 2016
Proficient Rx LP4powder, for suspension; tablet, film coatedGeneric drugs (ANDA)November 21, 2022
Sagent Pharmaceuticals4injection, powder, for solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 28, 2021
Shandong Anxin Pharmaceutical Co., Ltd.4injection, powder, for solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 14, 2023
American Health Packaging3tablet, film coatedGeneric drugs (ANDA)July 26, 2024
B. Braun Medical Inc.3injection, solutionNew drug applications (NDA)September 30, 2025
Baxter Healthcare Corporation3injection, solutionNew drug applications (NDA)April 1, 2023
BluePoint Laboratories3injection, powder, for solutionGeneric drugs (ANDA)August 11, 2021
Direct_Rx3tablet, film coated; powder, for suspensionGeneric drugs (ANDA)August 1, 2025
Hikma Pharmaceuticals USA Inc.3injection, powder, for solutionGeneric drugs (ANDA)December 22, 2009
Micro Labs Limited3tablet, film coatedGeneric drugs (ANDA)March 1, 2017
NorthStar RxLLC3injection, powder, for solutionGeneric drugs (ANDA)March 1, 2024
Roerig3injection, powder, for solutionNew drug applications (NDA)November 22, 1991
Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc.3injection, solutionNew drug applications (NDA)March 1, 1998
Advanced Rx of Tennessee, LLC2tablet, film coatedGeneric drugs (ANDA)March 3, 2023
Aurobindo Pharma Limited2powder, for suspensionGeneric drugs (ANDA)April 19, 2019
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)January 20, 2012
Coupler LLC2tablet, film coatedGeneric drugs (ANDA)May 7, 2026
Hawaii Repack, Inc.2powder, for suspensionGeneric drugs (ANDA)December 20, 2011
Medsource Pharmaceuticals2tablet, film coatedGeneric drugs (ANDA)March 1, 2017
Milla Pharmaceuticals Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 11, 2023
Northwind Health Company, LLC2tablet, film coatedGeneric drugs (ANDA)October 17, 2024
PD-Rx Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)October 31, 2002
PD-Rx Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)October 31, 2002
Redpharm Drug2for suspension; powder, for suspensionAuthorized generics (NDA)September 19, 2022
AbbVie Inc.1powder, for solutionNew drug applications (NDA)February 7, 2025
Allegis Holdings, LLC1for suspensionNew drug applications (NDA)September 1, 2023
Allergan, Inc.1powder, for solutionNew drug applications (NDA)December 26, 2014
Cipla USA Inc.1suspensionGeneric drugs (ANDA)October 28, 2024
Medical Purchasing Solutions, LLC1injection, powder, for solutionGeneric drugs (ANDA)February 10, 2012
Melinta Therapeutics, LLC1injection, powder, for solutionNew drug applications (NDA)October 2, 2017
Merck Sharp & Dohme LLC1injection, powder, for solutionNew drug applications (NDA)January 6, 2020
Merck Sharp & Dohme LLC1injection, powder, lyophilized, for solutionNew drug applications (NDA)December 19, 2014

Dosage forms

Dosage formProductsShare
Tablet, film coated11333.7%
Injection, powder, for solution8124.2%
Powder, for suspension5516.4%
Injection, powder, lyophilized, for solution3811.3%
Tablet133.9%
Injection, solution92.7%
For suspension72.1%
Suspension72.1%
Tablet, coated51.5%
Tablet, multilayer, extended release20.6%
Powder, for solution20.6%
Tablet, chewable20.6%

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.