"0006-5004-01" National Drug Code (NDC)

NDC Code	0006-5004-01
Package Description	1 VIAL, SINGLE-DOSE in 1 CARTON (0006-5004-01) / 24 mL in 1 VIAL, SINGLE-DOSE (0006-5004-02)
Product NDC	0006-5004
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Prevymis
Non-Proprietary Name	Letermovir
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20171108
Marketing Category Name	NDA
Application Number	NDA209940
Manufacturer	Merck Sharp & Dohme LLC
Substance Name	LETERMOVIR
Strength	20
Strength Unit	mg/mL
Pharmacy Classes	Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A Inhibitors [MoA], Cytomegalovirus DNA Terminase Complex Inhibitor [EPC], DNA Terminase Complex Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA]