"50242-923-01" National Drug Code (NDC)

NDC Code	50242-923-01
Package Description	1 VIAL, SINGLE-USE in 1 CARTON (50242-923-01) / 1 mL in 1 VIAL, SINGLE-USE
Product NDC	50242-923
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Hemlibra
Non-Proprietary Name	Emicizumab
Dosage Form	INJECTION, SOLUTION
Usage	SUBCUTANEOUS
Start Marketing Date	20171116
Marketing Category Name	BLA
Application Number	BLA761083
Manufacturer	Genentech, Inc.
Substance Name	EMICIZUMAB
Strength	150
Strength Unit	mg/mL