Minoxidil - 56062-798-16 - (Minoxidil)

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Drug Information of Minoxidil

Product NDC: 56062-798
Proprietary Name: Minoxidil
Non Proprietary Name: Minoxidil
Active Ingredient(s): 3    g/60mL & nbsp;   Minoxidil
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Minoxidil

Product NDC: 56062-798
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075598
Marketing Category: ANDA
Start Marketing Date: 20101025

Package Information of Minoxidil

Package NDC: 56062-798-16
Package Description: 1 BOTTLE in 1 CARTON (56062-798-16) > 60 mL in 1 BOTTLE

NDC Information of Minoxidil

NDC Code 56062-798-16
Proprietary Name Minoxidil
Package Description 1 BOTTLE in 1 CARTON (56062-798-16) > 60 mL in 1 BOTTLE
Product NDC 56062-798
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Minoxidil
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20101025
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name MINOXIDIL
Strength Number 3
Strength Unit g/60mL
Pharmaceutical Classes

Complete Information of Minoxidil


General Information