Minoxidil - 68084-205-01 - (Minoxidil)

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Drug Information of Minoxidil

Product NDC: 68084-205
Proprietary Name: Minoxidil
Non Proprietary Name: Minoxidil
Active Ingredient(s): 10    mg/1 & nbsp;   Minoxidil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Minoxidil

Product NDC: 68084-205
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071839
Marketing Category: ANDA
Start Marketing Date: 20070730

Package Information of Minoxidil

Package NDC: 68084-205-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-205-01) > 10 TABLET in 1 BLISTER PACK (68084-205-11)

NDC Information of Minoxidil

NDC Code 68084-205-01
Proprietary Name Minoxidil
Package Description 10 BLISTER PACK in 1 CARTON (68084-205-01) > 10 TABLET in 1 BLISTER PACK (68084-205-11)
Product NDC 68084-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minoxidil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070730
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name MINOXIDIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Minoxidil


General Information