Last Updated: May 10, 2026

Details for New Drug Application (NDA): 218175

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NDA 218175 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 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 suppliers are listed for this compound. Additional details are available on the minoxidil profile page.

Summary for 218175

Tradename:	MINOXIDIL (FOR WOMEN)
Applicant:	Taro
Ingredient:	minoxidil
Patents:	0

Pharmacology for NDA: 218175

Physiological Effect	Arteriolar Vasodilation

Medical Subject Heading (MeSH) Categories for 218175

Antihypertensive Agents
Vasodilator Agents

Suppliers and Packaging for NDA: 218175

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MINOXIDIL (FOR WOMEN)	minoxidil	SOLUTION;TOPICAL	218175	ANDA	SUN PHARMACEUTICAL INDUSTRIES, INC.	51672-2152	51672-2152-4	1 BOTTLE in 1 CARTON (51672-2152-4) / 60 mL in 1 BOTTLE
MINOXIDIL (FOR WOMEN)	minoxidil	SOLUTION;TOPICAL	218175	ANDA	SUN PHARMACEUTICAL INDUSTRIES, INC.	51672-2152	51672-2152-9	3 BOTTLE in 1 CARTON (51672-2152-9) / 60 mL in 1 BOTTLE

Profile for product number 001

Active Rx/OTC/Discontinued:	OTC	Dosage:	SOLUTION;TOPICAL			Strength	2%
Approval Date:	Nov 26, 2024	TE:		RLD:	No

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