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Data / Drug companies / Anthracycline Topoisomerase Inhibitor

Anthracycline Topoisomerase Inhibitor drugs: 7 drugs from 25 companies in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Anthracycline Topoisomerase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 86 products in this class from 25 companies, covering 7 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 5, 2026.

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  • 25Companies
  • 86Products
  • 7Drugs by generic name

Drugs in the Anthracycline Topoisomerase Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Doxorubicin hydrochloride6220
Idarubicin hydrochloride123
Daunorubicin hydrochloride63
Doxorubicin hydrochloride liposome21
Epirubicin hydrochloride21
(daunorubicin and cytarabine) liposome11
Doxorubicin11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hikma Pharmaceuticals USA Inc.18injection, solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 19, 2018
Pfizer Laboratories Div Pfizer Inc10injection, solutionNew drug applications (NDA)March 31, 2025
Baxter Healthcare Corporation7injection, suspension, liposomalNew drug applications (NDA)August 26, 2024
BluePoint Laboratories7injectable, liposomal; injection, suspension, liposomalGeneric drugs (ANDA)October 5, 2026
Meitheal Pharmaceuticals Inc.4injection, solutionGeneric drugs (ANDA)June 1, 2025
Gland Pharma Limited3injection, solutionGeneric drugs (ANDA)August 22, 2017
Hisun Pharmaceuticals USA, Inc.3injection, solutionGeneric drugs (ANDA)January 20, 2020
Pfizer Laboratories Div Pfizer Inc3solutionNew drug applications (NDA)February 17, 1997
Alembic Pharmaceuticals Inc.2injection, suspension, liposomalGeneric drugs (ANDA)June 27, 2025
Alembic Pharmaceuticals Limited2injection, suspension, liposomalGeneric drugs (ANDA)June 27, 2025
Amneal Pharmaceuticals LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 17, 2017
Dr. Reddy's Laboratories Inc.2injection, suspension, liposomalGeneric drugs (ANDA)June 27, 2025
Fresenius Kabi USA, LLC2injection, solutionGeneric drugs (ANDA)June 14, 2000
Lupin Pharmaceuticals, Inc.2injection, suspension, liposomalGeneric drugs (ANDA)August 26, 2024
NorthStar RxLLC2injectable, liposomalGeneric drugs (ANDA)May 29, 2019
Pharmacia & Upjohn Company LLC2injection, solutionNew drug applications (NDA)September 15, 1999
Qilu Pharmaceutical Co., Ltd.2injection, suspension, liposomalGeneric drugs (ANDA)February 3, 2026
Sagent Pharmaceuticals2injection, suspension, liposomal; injection, solutionGeneric drugs (ANDA)March 1, 2026
Sun Pharmaceutical Industries, Inc.2injection, solutionGeneric drugs (ANDA)February 20, 2012
Sun Pharmaceutical Industries, Inc.2injectable, liposomalGeneric drugs (ANDA)February 5, 2013
Zydus Lifesciences Limited2injectable, liposomalGeneric drugs (ANDA)September 14, 2020
Zydus Pharmaceuticals USA Inc.2injectable, liposomalGeneric drugs (ANDA)September 14, 2020
Actavis Pharma, Inc.1injection, solutionGeneric drugs (ANDA)November 1, 2014
Jazz Pharmaceuticals, Inc.1injection, powder, lyophilized, for suspensionNew drug applications (NDA)August 3, 2017
Mylan Institutional LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 27, 2014

Dosage forms

Dosage formProductsShare
Injection, solution4248.8%
Injection, suspension, liposomal2124.4%
Injectable, liposomal1214%
Injection, powder, lyophilized, for solution55.8%
Solution33.5%
Injection22.3%
Injection, powder, lyophilized, for suspension11.2%

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.