"42358-475-30" National Drug Code (NDC)

NDC Code	42358-475-30
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (42358-475-30) / 30 CAPSULE in 1 BOTTLE, PLASTIC
Product NDC	42358-475
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zokinvy
Non-Proprietary Name	Lonafarnib
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20250702
Marketing Category Name	NDA
Application Number	NDA213969
Manufacturer	Sentynl Therapeutics, Inc.
Substance Name	LONAFARNIB
Strength	75
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Farnesyltransferase Inhibitor [EPC], Farnesyltransferase Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]