"72064-125-30" National Drug Code (NDC)

NDC Code	72064-125-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72064-125-30)
Product NDC	72064-125
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ayvakit
Non-Proprietary Name	Avapritinib
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20210616
Marketing Category Name	NDA
Application Number	NDA212608
Manufacturer	Blueprint Medicines Corporation
Substance Name	AVAPRITINIB
Strength	25
Strength Unit	mg/1
Pharmacy Classes	Bile Salt Export Pump Inhibitors [MoA], Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Kinase Inhibitor [EPC], Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA], Multidrug and Toxin Extrusion Transporter 2 K Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], Tyrosine Kinase Inhibitors [MoA]