"31722-779-33" National Drug Code (NDC)

NDC Code	31722-779-33
Package Description	4 BLISTER PACK in 1 CARTON (31722-779-33) / 28 CAPSULE in 1 BLISTER PACK
Product NDC	31722-779
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nilotinib
Non-Proprietary Name	Nilotinib
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20251119
Marketing Category Name	ANDA
Application Number	ANDA209651
Manufacturer	Camber Pharmaceuticals, Inc.
Substance Name	NILOTINIB
Strength	150
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]