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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 075357

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NDA 075357 describes MINOXIDIL (FOR WOMEN), which is a drug marketed by Aurobindo Pharma, P And L, Taro, Apotex Inc, Aurobindo Pharma Ltd, Hikma, L Perrigo Co, and Sight Pharms, and is included in nine NDAs. It is available from thirty-four suppliers. Additional details are available on the MINOXIDIL (FOR WOMEN) profile page.

The generic ingredient in MINOXIDIL (FOR WOMEN) is minoxidil. There are eight drug master file entries for this compound. Eighty-six suppliers are listed for this compound. Additional details are available on the minoxidil profile page.

Summary for 075357

Tradename:	MINOXIDIL (FOR WOMEN)
Applicant:	L Perrigo Co
Ingredient:	minoxidil
Patents:	0

Pharmacology for NDA: 075357

Physiological Effect	Arteriolar Vasodilation

Medical Subject Heading (MeSH) Categories for 075357

Antihypertensive Agents
Vasodilator Agents

Suppliers and Packaging for NDA: 075357

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MINOXIDIL (FOR MEN)	minoxidil	SOLUTION;TOPICAL	075357	ANDA	L. Perrigo Company	0113-6500	0113-6500-00	3 BOTTLE in 1 CARTON (0113-6500-00) / 60 mL in 1 BOTTLE (0113-6500-30)
MINOXIDIL (FOR MEN)	minoxidil	SOLUTION;TOPICAL	075357	ANDA	Walgreen Company	0363-0703	0363-0703-16	1 BOTTLE, DROPPER in 1 CARTON (0363-0703-16) / 60 mL in 1 BOTTLE, DROPPER

Profile for product number 001

Active Rx/OTC/Discontinued:	OTC	Dosage:	SOLUTION;TOPICAL			Strength	2%
Approval Date:	Jul 30, 1999	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	OTC	Dosage:	SOLUTION;TOPICAL			Strength	2%
Approval Date:	Jul 30, 1999	TE:		RLD:	No

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