"72301-595-10" National Drug Code (NDC)

NDC Code	72301-595-10
Package Description	1 VIAL in 1 CARTON (72301-595-10) / 1 POWDER in 1 VIAL
Product NDC	72301-595
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Jeuveau
Non-Proprietary Name	Prabotulinum Toxin Type A
Dosage Form	POWDER
Usage	INTRAMUSCULAR
Start Marketing Date	20190213
Marketing Category Name	BLA
Application Number	BLA761085
Manufacturer	Evolus, Inc.
Substance Name	BOTULINUM TOXIN TYPE A
Strength	100
Strength Unit	[USP'U]/1
Pharmacy Classes	Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC]