"65597-402-20" National Drug Code (NDC)

NDC Code	65597-402-20
Package Description	1 BOTTLE in 1 CARTON (65597-402-20) / 120 CAPSULE in 1 BOTTLE
Product NDC	65597-402
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Turalio
Non-Proprietary Name	Pexidartinib
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20190802
End Marketing Date	20240131
Marketing Category Name	NDA
Application Number	NDA211810
Manufacturer	Daiichi Sankyo Inc.
Substance Name	PEXIDARTINIB HYDROCHLORIDE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Colony Stimulating Factor Receptor Type 1 (CSF-1R) Inhibitors [MoA], Cytochrome P450 2B6 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Kinase Inhibitor [EPC], Kinase Inhibitors [MoA], Tyrosine Kinase Inhibitors [MoA], UGT1A1 Inhibitors [MoA]