"72934-4074-8" National Drug Code (NDC)

NDC Code	72934-4074-8
Package Description	60 g in 1 BOTTLE, GLASS (72934-4074-8)
Product NDC	72934-4074
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Finasteride 0.1% / Minoxidil 5%
Non-Proprietary Name	Finasteride 0.1% / Minoxidil 5%
Dosage Form	SOLUTION
Usage	TOPICAL
Start Marketing Date	20190509
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Sincerus Florida, LLC
Substance Name	MINOXIDIL; FINASTERIDE
Strength	5; .1
Strength Unit	g/100g; g/100g
Pharmacy Classes	Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]