"73207-101-31" National Drug Code (NDC)

NDC Code	73207-101-31
Package Description	1 BOTTLE in 1 CARTON (73207-101-31) / 30 TABLET in 1 BOTTLE
Product NDC	73207-101
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Qinlock
Non-Proprietary Name	Ripretinib
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200515
Marketing Category Name	NDA
Application Number	NDA213973
Manufacturer	Deciphera Pharmaceuticals, LLC
Substance Name	RIPRETINIB
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA], Platelet-derived Growth Factor alpha Receptor Inhibitors [MoA], Stem Cell Factor (KIT) Receptor Inhibitors [MoA]