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Serving hundreds of leading biopharmaceutical companies globally:

US Department of Justice
Chinese Patent Office
US Army
Argus Health

Generated: March 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072708

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NDA 072708 describes MINOXIDIL, which is a drug marketed by Perrigo Israel, Mutual Pharm, Par Pharm, Royce Labs, Sun Pharm Industries, Usl Pharma, Watson Labs, Watson Labs Inc, Actavis Mid Atlantic, Apotex Inc, Bausch And Lomb, Copley Pharm, Hi Tech Pharma, L Perrigo Co, Sight Pharms, Teva, Wockhardt Bio Ag, Avacor Prods, Perrigo, and Perrigo New York, and is included in twenty-six NDAs. It is available from thirty 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. Fifty-four suppliers are listed for this compound. Additional details are available on the minoxidil profile page.
Summary for 072708
Applicant:Mutual Pharm
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 072708
Physiological EffectArteriolar Vasodilation
Medical Subject Heading (MeSH) Categories for 072708
Suppliers and Packaging for NDA: 072708
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MINOXIDIL minoxidil TABLET;ORAL 072708 ANDA AvKARE, Inc. 42291-618 N 42291-618-90
MINOXIDIL minoxidil TABLET;ORAL 072708 ANDA AvKARE, Inc. 42291-618 N 42291-618-01

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength2.5MG
Approval Date:Dec 14, 1995TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Daiichi Sankyo
Argus Health

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