Drugplain

VANFLYTA 26.5 mg/1

QUIZARTINIB · TABLET, FILM COATED · Daiichi Sankyo Inc.

No Recall History
Plain English

Vanflyta (quizartinib) is an oral tablet used to treat acute myeloid leukemia in certain adult patients. It works by targeting specific mutations in cancer cells to help stop their growth.

Key Facts

Brand Name
VANFLYTA
Generic Name
QUIZARTINIB
NDC Code (Product)
65597-511
Manufacturer
Daiichi Sankyo Inc.
Strength
26.5 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA216993
Marketing Start
07/20/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

off label use65 reports
no adverse event57 reports
death49 reports
nausea38 reports
platelet count decreased38 reports
pyrexia36 reports
infection32 reports
febrile neutropenia31 reports
electrocardiogram qt prolonged29 reports
disease progression26 reports

Frequently Asked Questions

What is VANFLYTA used for?

Vanflyta (quizartinib) is an oral tablet used to treat acute myeloid leukemia in certain adult patients. It works by targeting specific mutations in cancer cells to help stop their growth.

Is VANFLYTA a controlled substance?

VANFLYTA is not classified as a controlled substance by the DEA.

What is the generic name for VANFLYTA?

The generic name for VANFLYTA is QUIZARTINIB. There are no other listed brand versions of QUIZARTINIB.

What is the NDC code for VANFLYTA 26.5 mg/1?

The NDC (National Drug Code) for VANFLYTA 26.5 mg/1 is 65597-511, listed by Daiichi Sankyo Inc..

Product NDC

65597-511

Package NDC

65597-511-04

Other VANFLYTA Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)