"13668-711-91" National Drug Code (NDC)

NDC Code	13668-711-91
Package Description	1 BLISTER PACK in 1 CARTON (13668-711-91) / 28 CAPSULE in 1 BLISTER PACK
Product NDC	13668-711
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nilotinib
Non-Proprietary Name	Nilotinib
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20251216
Marketing Category Name	ANDA
Application Number	ANDA218532
Manufacturer	Torrent Pharmaceuticals Limited
Substance Name	NILOTINIB HYDROCHLORIDE MONOHYDRATE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA], UGT1A1 Inhibitors [MoA]