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Data / Drug companies / Proteasome Inhibitor

Proteasome Inhibitor drugs: 3 drugs from 27 companies in the FDA NDC directory

Proteasome Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 39 products in this class from 27 companies, covering 3 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on May 1, 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.

  • 27Companies
  • 39Products
  • 3Drugs by generic name

Drugs in the Proteasome Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Bortezomib3326
Carfilzomib31
Ixazomib31

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Takeda Pharmaceuticals America, Inc.4capsule; injection, powder, lyophilized, for solutionNew drug applications (NDA)November 20, 2015
BluePoint Laboratories3injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 31, 2022
Hospira, Inc.3injection, powder, lyophilized, for solutionNew drug applications (NDA)July 27, 2022
Onyx Pharmaceuticals, Inc.3injection, powder, lyophilized, for solutionNew drug applications (NDA)May 23, 2018
Eugia US LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Gland Pharma Limited2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 6, 2026
Maia Pharmaceuticals, Inc.2injectionNew drug applications (NDA)August 11, 2022
Amneal Pharmaceuticals LLC1injectionNew drug applications (NDA)September 27, 2024
Apotex Corp.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Avenacy, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 1, 2026
Camber Pharmaceuticals, Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 3, 2024
Dr. Reddy's Laboratories Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 26, 2022
Fresenius Kabi USA, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Hikma Pharmaceuticals USA Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 27, 2022
Meitheal Pharmaceuticals Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 26, 2022
Ningbo Shuangcheng Pharmaceutical Co., Ltd1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 17, 2025
NorthStar RxLLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)November 1, 2024
Novadoz Pharmaceuticals LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 26, 2022
Pharmascience Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Qilu Pharmaceutical Co., Ltd.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Sagent Pharmaceuticals1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 15, 2025
Shilpa Medicare Limited1injectionNew drug applications (NDA)September 25, 2024
Sintetica US LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 15, 2023
Somerset Therapeutics, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 29, 2025
Waverley Pharma Inc1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 19, 2018
Zydus Lifesciences Limited1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022
Zydus Pharmaceuticals USA Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 2, 2022

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution3282.1%
Injection410.3%
Capsule37.7%

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.