"72934-4748-8" National Drug Code (NDC)

NDC Code	72934-4748-8
Package Description	60 g in 1 BOTTLE, GLASS (72934-4748-8)
Product NDC	72934-4748
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Minoxidil 7% / Progesterone 0.1%
Non-Proprietary Name	Minoxidil 7% / Progesterone 0.1%
Dosage Form	SOLUTION
Usage	TOPICAL
Start Marketing Date	20190501
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Sincerus Florida, LLC
Substance Name	MINOXIDIL; PROGESTERONE
Strength	7; .1
Strength Unit	g/100g; g/100g
Pharmacy Classes	Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],Progesterone [CS],Progesterone [EPC]