"42388-025-57" National Drug Code (NDC)

NDC Code	42388-025-57
Package Description	1 BOTTLE in 1 CARTON (42388-025-57) / 15 TABLET in 1 BOTTLE
Product NDC	42388-025
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cabometyx
Non-Proprietary Name	Cabozantinib
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20160425
Marketing Category Name	NDA
Application Number	NDA208692
Manufacturer	Exelixis, Inc.
Substance Name	CABOZANTINIB S-MALATE
Strength	40
Strength Unit	mg/1
Pharmacy Classes	Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]