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Data / Drug companies / Microtubule Inhibitor

Microtubule Inhibitor drugs: 7 drugs from 50 companies in the FDA NDC directory

Microtubule Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 133 products in this class from 50 companies, covering 7 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 19, 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.

  • 50Companies
  • 133Products
  • 7Drugs by generic name

Drugs in the Microtubule Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Docetaxel5621
Paclitaxel4120
Eribulin mesylate1817
Docetaxel anhydrous145
Paclitaxel protein-bound particles22
Paclitaxel (aibumin-bound)11
Tirbanibulin11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hospira, Inc.11injection, solutionNew drug applications (NDA)January 10, 2022
Gland Pharma Limited7injection; injection, solutionGeneric drugs (ANDA)April 5, 2024
Teva Parenteral Medicines, Inc.7injection, solution, concentrateGeneric drugs (ANDA)July 7, 2020
Baxter Healthcare Corporation6injection, solution; injectionNew drug applications (NDA)November 27, 2025
Dr. Reddy's Laboratories Inc.6injection, solution; injectionGeneric drugs (ANDA)January 22, 2026
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.6injection, solution; injectionGeneric drugs (ANDA)December 15, 2024
Meitheal Pharmaceuticals Inc.5injection, solution, concentrate; injectionGeneric drugs (ANDA)October 19, 2026
Mylan Institutional LLC5injection, solution; injection, solution, concentrateGeneric drugs (ANDA)October 9, 2025
Alembic Pharmaceuticals Inc.4injectionGeneric drugs (ANDA)February 28, 2023
Alembic Pharmaceuticals Limited4injectionGeneric drugs (ANDA)February 28, 2023
BluePoint Laboratories4solution; injectionGeneric drugs (ANDA)April 1, 2026
Amneal Pharmaceuticals LLC3injectionGeneric drugs (ANDA)January 19, 2018
Avyxa Pharma, LLC3injection, solutionNew drug applications (NDA)May 9, 2024
Eugia US LLC3injection, solutionGeneric drugs (ANDA)June 25, 2021
Hikma Pharmaceuticals USA Inc.3injection, solution, concentrate; injectionGeneric drugs (ANDA)June 28, 2024
Jiangsu Hengrui Pharmaceuticals Co., Ltd.3injection, solution, concentrateGeneric drugs (ANDA)August 9, 2017
Mylan Institutional LLC3injection, solutionGeneric drugs (ANDA)August 3, 2022
Natco Pharma USA LLC3injection, solutionGeneric drugs (ANDA)November 7, 2024
Novadoz Pharmaceuticals LLC3injection, solutionGeneric drugs (ANDA)August 26, 2020
Sagent Pharmaceuticals3injection, solution; injectionGeneric drugs (ANDA)February 1, 2024
Sanofi-Aventis U.S. LLC3injection, solution, concentrateAuthorized generics (NDA)October 23, 2016
Sun Pharmaceutical Industries, Inc.3injection, solutionNew drug applications (NDA)November 26, 2020
Actavis Pharma, Inc.2injection, solution, concentrateNew drug applications (NDA)September 1, 2014
Apotex Corp.2injectionGeneric drugs (ANDA)March 19, 2025
Hospira, Inc.2injection, solutionGeneric drugs (ANDA)April 8, 2025
NorthStar RxLLC2solution; injection, powder, lyophilized, for suspensionGeneric drugs (ANDA)December 5, 2025
Sandoz Inc2injection, powder, lyophilized, for suspension; injectionGeneric drugs (ANDA)July 7, 2025
Zhuhai Beihai Biotech Co., Ltd.2injection, solutionNew drug applications (NDA)December 15, 2025
Zydus Pharmaceuticals USA Inc.2injection, solutionNew drug applications (NDA)December 15, 2025
Abraxis BioScience, LLC1injection, powder, lyophilized, for suspensionNew drug applications (NDA)February 10, 2005
Accord Healthcare Inc.1injection, solution, concentrateNew drug applications (NDA)May 30, 2013
Almirall, LLC1ointmentNew drug applications (NDA)December 14, 2020
American Regent, Inc.1injection, powder, lyophilized, for suspensionNew drug applications (NDA)May 2, 2023
BSP Pharmaceuticals S.p.A.1injectionNew drug applications (NDA)April 21, 2017
Baxter Healthcare Company1injectionGeneric drugs (ANDA)October 1, 2024
Bryant Ranch Prepack1injection, solutionGeneric drugs (ANDA)August 26, 2020
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.1injectionGeneric drugs (ANDA)March 4, 2025
Cipla USA Inc.1injection, powder, lyophilized, for suspensionGeneric drugs (ANDA)April 15, 2025
Eisai Inc.1injectionNew drug applications (NDA)November 15, 2010
Exelan Pharmaceuticals Inc.1injection, powder, lyophilized, for suspensionGeneric drugs (ANDA)August 11, 2026
Fresenius Kabi USA, LLC1injection, solutionGeneric drugs (ANDA)March 20, 2009
Glenmark Pharmaceuticals Inc., USA1injectionGeneric drugs (ANDA)August 5, 2025
Kindos Pharmaceuticals Co., Ltd.1injectionGeneric drugs (ANDA)August 5, 2025
Long Grove Pharmaceuticals, LLC1solutionGeneric drugs (ANDA)July 22, 2024
Ningbo Shuangcheng Pharmaceutical Co., Ltd1injection, powder, lyophilized, for suspensionGeneric drugs (ANDA)May 15, 2025
NorthStar Rx LLC1injection, solutionGeneric drugs (ANDA)January 25, 2021
Sandoz Inc1injection, solutionNew drug applications (NDA)June 29, 2011
Sun Pharmaceutical Industries, Inc.1injectionGeneric drugs (ANDA)May 15, 2025
Teva Pharmaceuticals, Inc.1injection, powder, lyophilized, for suspensionNew drug applications (NDA)July 2, 2024
XGen Pharmaceuticals DJB, Inc.1injectionGeneric drugs (ANDA)April 7, 2026

Dosage forms

Dosage formProductsShare
Injection, solution6045.1%
Injection3727.8%
Injection, solution, concentrate2115.8%
Injection, powder, lyophilized, for suspension118.3%
Solution32.3%
Ointment10.8%

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.