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Womens Rogaine - 42002-105-06 - (Minoxidil)

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Drug Information of Womens Rogaine

Product NDC: 42002-105
Proprietary Name: Womens Rogaine
Non Proprietary Name: Minoxidil
Active Ingredient(s): 20    mg/mL & nbsp;   Minoxidil
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Womens Rogaine

Product NDC: 42002-105
Labeler Name: Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019501
Marketing Category: NDA
Start Marketing Date: 20100801

Package Information of Womens Rogaine

Package NDC: 42002-105-06
Package Description: 3 BOTTLE, PLASTIC in 1 CARTON (42002-105-06) > 60 mL in 1 BOTTLE, PLASTIC

NDC Information of Womens Rogaine

NDC Code 42002-105-06
Proprietary Name Womens Rogaine
Package Description 3 BOTTLE, PLASTIC in 1 CARTON (42002-105-06) > 60 mL in 1 BOTTLE, PLASTIC
Product NDC 42002-105
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Minoxidil
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20100801
Marketing Category Name NDA
Labeler Name Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance Name MINOXIDIL
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Womens Rogaine


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