NDC 65597-504 – Vanflyta

Quizartinib Dihydrochloride 17.7 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65597-504

Product details

Brand name
Vanflyta
Generic name
Quizartinib
Labeler
Daiichi Sankyo Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA216993
Marketed since
July 20, 2023
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Vanflyta →

Package NDC codes (2)

Package NDCDescriptionSince
65597-504-041 BOTTLE in 1 CARTON (65597-504-04) / 14 TABLET, FILM COATED in 1 BOTTLEJul 20, 2023
65597-504-281 BOTTLE in 1 CARTON (65597-504-28) / 28 TABLET, FILM COATED in 1 BOTTLEJul 20, 2023

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