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Up and Up minoxidil - 11673-856-30 - (Minoxidil)

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Drug Information of Up and Up minoxidil

Product NDC: 11673-856
Proprietary Name: Up and Up 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 Up and Up minoxidil

Product NDC: 11673-856
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075357
Marketing Category: ANDA
Start Marketing Date: 20090527

Package Information of Up and Up minoxidil

Package NDC: 11673-856-30
Package Description: 3 BOTTLE in 1 CARTON (11673-856-30) > 60 mL in 1 BOTTLE

NDC Information of Up and Up minoxidil

NDC Code 11673-856-30
Proprietary Name Up and Up minoxidil
Package Description 3 BOTTLE in 1 CARTON (11673-856-30) > 60 mL in 1 BOTTLE
Product NDC 11673-856
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Minoxidil
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20090527
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name MINOXIDIL
Strength Number 2
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Up and Up minoxidil


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