Friday, July 10, 2026

Drug profile · INN

quizartinib dihydrochloride

quizartinib dihydrochloride (VANFLYTA) is a tyrosine-protein kinase receptor flt3 inhibitor. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — quizartinib dihydrochloride
US status
approved
Class
Route
ORAL
Patents
0
Programs
0
Data quality
0.84

Quick answer

quizartinib dihydrochloride (VANFLYTA) is a tyrosine-protein kinase receptor flt3 inhibitor. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN quizartinib dihydrochloride
Brand VANFLYTA
Mechanism Tyrosine-protein kinase receptor FLT3 inhibitor
Target Receptor-type tyrosine-protein kinase FLT3
Route ORAL
Formulation TABLET

Mechanism of action

Tyrosine-protein kinase receptor FLT3 inhibitor

Primary target: Receptor-type tyrosine-protein kinase FLT3

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. gilteritinib fumarate Tyrosine-protein kinase receptor FLT3 inhibitor
  2. gilteritinib Antineoplastic and immunomodulating agents (L01)
  3. quizartinib hydrochloride Tyrosine-protein kinase receptor FLT3 inhibitor

Frequently asked questions

What is quizartinib dihydrochloride?

quizartinib dihydrochloride (VANFLYTA) is a tyrosine-protein kinase receptor flt3 inhibitor. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for quizartinib dihydrochloride?

VANFLYTA is a marketed brand name for quizartinib dihydrochloride. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of quizartinib dihydrochloride?

quizartinib dihydrochloride 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.