"51144-002-12" National Drug Code (NDC)

NDC Code	51144-002-12
Package Description	120 TABLET in 1 BOTTLE (51144-002-12)
Product NDC	51144-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tukysa
Non-Proprietary Name	Tucatinib
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200417
Marketing Category Name	NDA
Application Number	NDA213411
Manufacturer	SEAGEN INC.
Substance Name	TUCATINIB
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA], Tyrosine Kinase Inhibitors [MoA]