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Last Updated: March 26, 2025

Details for New Drug Application (NDA): 071799

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NDA 071799 describes MINOXIDIL, which is a drug marketed by Perrigo Pharma Intl, Endo Operations, Royce Labs, Sun Pharm Industries, Usl Pharma, Watson Labs, Aurobindo Pharma, P And L, Taro, Apotex Inc, Aurobindo Pharma Ltd, Bausch And Lomb, Copley Pharm, Hikma, L Perrigo Co, Sight Pharms, Teva, Avacor Prods, Perrigo, and Perrigo New York, and is included in twenty-eight NDAs. It is available from twenty-nine suppliers. Additional details are available on the MINOXIDIL profile page.

The generic ingredient in MINOXIDIL 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 071799

Tradename:	MINOXIDIL
Applicant:	Royce Labs
Ingredient:	minoxidil
Patents:	0

Medical Subject Heading (MeSH) Categories for 071799

Antihypertensive Agents
Vasodilator Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	2.5MG
Approval Date:	Nov 10, 1987	TE:		RLD:	No

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