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Data / Drug companies / Cytoprotective Agent

Cytoprotective Agent drugs: 7 drugs from 18 companies in the FDA NDC directory

Cytoprotective Agent is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 35 products in this class from 18 companies, covering 7 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on March 16, 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.

  • 18Companies
  • 35Products
  • 7Drugs by generic name

Drugs in the Cytoprotective Agent class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Mesna119
Bleomycin84
Dexrazoxane for injection63
Dexrazoxane43
Bleomycin sulfate42
Amifostine11
Mesna injection11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hikma Pharmaceuticals USA Inc.5injection, powder, lyophilized, for solution; injection, solutionGeneric drugs (ANDA)January 9, 2018
Fresenius Kabi USA, LLC3injection, powder, lyophilized, for solution; injection, solutionGeneric drugs (ANDA)February 13, 2009
Gland Pharma Limited3injection, powder, lyophilized, for solution; solutionGeneric drugs (ANDA)December 16, 2019
Almaject, Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 1, 2022
Baxter Healthcare Company2injection, solutionNew drug applications (NDA)December 30, 1988
Baxter Healthcare Corporation2injection, solutionNew drug applications (NDA)December 30, 1988
Fosun Pharma USA Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)November 1, 2021
Hospira, Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 25, 2018
Hospira, Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 11, 2000
Meitheal Pharmaceuticals Inc.2powder, for solutionGeneric drugs (ANDA)August 31, 2018
NorthStar Rx LLC2powder, for solutionGeneric drugs (ANDA)December 1, 2018
Novadoz Pharmaceuticals LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 26, 2025
Bamboo US Bidco LCC1injection, solutionNew drug applications (NDA)December 30, 1988
Baxter Healthcare Company1tablet, film coatedNew drug applications (NDA)March 21, 2002
Eugia US LLC1injection, solutionGeneric drugs (ANDA)January 27, 2026
Ingenus Pharmaceuticals, LLC1tablet, film coatedGeneric drugs (ANDA)January 14, 2025
Legacy Pharma USA Inc.1injectionNew drug applications (NDA)March 16, 2026
Sagent Pharmaceuticals1injection, solutionGeneric drugs (ANDA)December 1, 2010

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution1851.4%
Injection, solution925.7%
Powder, for solution411.4%
Tablet, film coated25.7%
Injection12.9%
Solution12.9%

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.