Minoxidil - 49349-654-02 - (Minoxidil)

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Drug Information of Minoxidil

Product NDC: 49349-654
Proprietary Name: Minoxidil
Non Proprietary Name: Minoxidil
Active Ingredient(s): 2.5    mg/1 & nbsp;   Minoxidil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Minoxidil

Product NDC: 49349-654
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071826
Marketing Category: ANDA
Start Marketing Date: 20110518

Package Information of Minoxidil

Package NDC: 49349-654-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-654-02)

NDC Information of Minoxidil

NDC Code 49349-654-02
Proprietary Name Minoxidil
Package Description 30 TABLET in 1 BLISTER PACK (49349-654-02)
Product NDC 49349-654
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minoxidil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110518
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name MINOXIDIL
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Minoxidil


General Information