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Generated: April 28, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072708

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NDA 072708 describes MINOXIDIL, which is a drug marketed by Mutual Pharm, Sun Pharm Inds, Par Pharm, Usl Pharma, Perrigo Israel, Watson Labs, Royce Labs, Copley Pharm, Apotex Inc, Hi Tech Pharma, Bausch And Lomb, Sight Pharms, Perrigo, Wockhardt, Actavis Mid Atlantic, Teva, Watson Labs Inc, Avacor Prods, 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-five suppliers are listed for this compound. Additional details are available on the minoxidil profile page.

Summary for NDA: 072708

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:1
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 072708

Physiological EffectArteriolar Vasodilation

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 42291-618-01 100 TABLET in 1 BOTTLE (42291-618-01)
MINOXIDIL
minoxidil
TABLET;ORAL 072708 ANDA AvKARE, Inc. 42291-618 42291-618-90 90 TABLET in 1 BOTTLE (42291-618-90)

Summary for product number 001

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


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