Saturday, July 11, 2026

Drug profile · INN

ibritumomab tiuxetan

ibritumomab tiuxetan (ZEVALIN) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

FDA: approved EMA: unknown Various (V10) V10XX02
US status approved
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Drug details — ibritumomab tiuxetan
US status
approved
Class
Various (V10)
Route
INJECTION
Patents
0
Programs
0
Data quality
0.84

Quick answer

ibritumomab tiuxetan (ZEVALIN) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN ibritumomab tiuxetan
Brand ZEVALIN
Mechanism B-lymphocyte antigen CD20 binding agent
Therapeutic class Various (V10)
Route INJECTION
Formulation INJECTABLE
ATC code V10XX02

Mechanism of action

B-lymphocyte antigen CD20 binding agent

Approval history

Authority Status Date
FDA approved
EMA unknown

Related & competitor drugs

  1. besilesomab Various (V09)
  2. deferasirox Various (V03)
  3. ferric citrate coordination complex Various (V03)
  4. folic acid Various (V04)
  5. sevelamer carbonate Various (V03)
  6. sugammadex sodium Various (V03)

Frequently asked questions

What is ibritumomab tiuxetan?

ibritumomab tiuxetan (ZEVALIN) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for ibritumomab tiuxetan?

ZEVALIN is a marketed brand name for ibritumomab tiuxetan. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of ibritumomab tiuxetan?

ibritumomab tiuxetan has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.