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Last Updated: November 4, 2024

Details for New Drug Application (NDA): 071796

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NDA 071796 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-seven 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. One hundred and five suppliers are listed for this compound. Additional details are available on the minoxidil profile page.

Summary for 071796

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

Medical Subject Heading (MeSH) Categories for 071796

Antihypertensive Agents
Vasodilator Agents

Profile for product number 001

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

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