"42388-025-26" National Drug Code (NDC)

NDC Code	42388-025-26
Package Description	30 TABLET in 1 BOTTLE (42388-025-26)
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]