"59676-225-07" National Drug Code (NDC)

NDC Code	59676-225-07
Package Description	7 CAPSULE in 1 BOTTLE (59676-225-07)
Product NDC	59676-225
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olysio
Non-Proprietary Name	Simeprevir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20131122
Marketing Category Name	NDA
Application Number	NDA205123
Manufacturer	Janssen Products LP
Substance Name	SIMEPREVIR
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Hepatitis C Virus NS3/4A Protease Inhibitor [EPC],HCV NS3/4A Protease Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA],Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA]