MINOXIDIL - 54868-3467-1 - (Minoxidil)

Alphabetical Index


Drug Information of MINOXIDIL

Product NDC: 54868-3467
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: 54868-3467
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071345
Marketing Category: ANDA
Start Marketing Date: 19960913

Package Information of MINOXIDIL

Package NDC: 54868-3467-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-3467-1)

NDC Information of MINOXIDIL

NDC Code 54868-3467-1
Proprietary Name MINOXIDIL
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-3467-1)
Product NDC 54868-3467
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minoxidil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960913
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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