MINOXIDIL - 53489-387-03 - (minoxidil)

Alphabetical Index


Drug Information of MINOXIDIL

Product NDC: 53489-387
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: 53489-387
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072709
Marketing Category: ANDA
Start Marketing Date: 19951214

Package Information of MINOXIDIL

Package NDC: 53489-387-03
Package Description: 250 TABLET in 1 BOTTLE (53489-387-03)

NDC Information of MINOXIDIL

NDC Code 53489-387-03
Proprietary Name MINOXIDIL
Package Description 250 TABLET in 1 BOTTLE (53489-387-03)
Product NDC 53489-387
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name minoxidil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19951214
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, 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