Minoxidil - 52125-039-02 - (Minoxidil)

Alphabetical Index


Drug Information of Minoxidil

Product NDC: 52125-039
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: 52125-039
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071839
Marketing Category: ANDA
Start Marketing Date: 20130226

Package Information of Minoxidil

Package NDC: 52125-039-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-039-02)

NDC Information of Minoxidil

NDC Code 52125-039-02
Proprietary Name Minoxidil
Package Description 30 TABLET in 1 BLISTER PACK (52125-039-02)
Product NDC 52125-039
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minoxidil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130226
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name MINOXIDIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Minoxidil


General Information