Skip to the page

Data / Drug companies / Ifosfamide

Ifosfamide: 5 companies and 11 products in the FDA NDC directory

Ifosfamide is listed in the FDA National Drug Code Directory by 5 companies, with 11 products in commercial distribution. 5 of the products (45.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, for solution; injection; injection, solution, and the newest product started marketing on June 10, 2017.

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.

Companies listing it
5
Products
11
Generic (ANDA) products
5 (45.5%)
Application numbers
4
Routes
Intravenous
Brand names
Ifex
openFDA record search
api.fda.gov

Companies that list ifosfamide

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Baxter Healthcare Company4injection, powder, for solutionNew drug applications (NDA)December 30, 1988
Baxter Healthcare Corporation2injection, powder, for solutionNew drug applications (NDA)December 30, 1988
Hikma Pharmaceuticals USA Inc.2injectionGeneric drugs (ANDA)June 10, 2017
Meitheal Pharmaceuticals Inc.2injection, solutionGeneric drugs (ANDA)July 26, 2007
Fresenius Kabi USA, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 28, 2003

Dosage forms

Dosage formProductsShare
Injection, powder, for solution654.5%
Injection218.2%
Injection, solution218.2%
Injection, powder, lyophilized, for solution19.1%

Marketing categories

Marketing categoryProductsShare
New drug applications (NDA)654.5%
Generic drugs (ANDA)545.5%

Pharmacologic classes

ClassProducts
Alkylating Drug11

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.