Minoxidil - 54868-3781-1 - (minoxidil)

Alphabetical Index


Drug Information of Minoxidil

Product NDC: 54868-3781
Proprietary Name: Minoxidil
Non Proprietary Name: minoxidil
Active Ingredient(s): 2    g/100mL & nbsp;   minoxidil
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Minoxidil

Product NDC: 54868-3781
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074588
Marketing Category: ANDA
Start Marketing Date: 19960604

Package Information of Minoxidil

Package NDC: 54868-3781-1
Package Description: 1 BOTTLE in 1 CARTON (54868-3781-1) > 60 mL in 1 BOTTLE

NDC Information of Minoxidil

NDC Code 54868-3781-1
Proprietary Name Minoxidil
Package Description 1 BOTTLE in 1 CARTON (54868-3781-1) > 60 mL in 1 BOTTLE
Product NDC 54868-3781
Product Type Name HUMAN OTC DRUG
Non Proprietary Name minoxidil
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19960604
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MINOXIDIL
Strength Number 2
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Minoxidil


General Information