Product NDC: | 42002-106 |
Proprietary Name: | Mens rogaine |
Non Proprietary Name: | Minoxidil |
Active Ingredient(s): | 50 mg/g & nbsp; Minoxidil |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42002-106 |
Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021812 |
Marketing Category: | NDA |
Start Marketing Date: | 20101001 |
Package NDC: | 42002-106-11 |
Package Description: | 1 CAN in 1 PACKAGE (42002-106-11) > 60 g in 1 CAN |
NDC Code | 42002-106-11 |
Proprietary Name | Mens rogaine |
Package Description | 1 CAN in 1 PACKAGE (42002-106-11) > 60 g in 1 CAN |
Product NDC | 42002-106 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Minoxidil |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20101001 |
Marketing Category Name | NDA |
Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
Substance Name | MINOXIDIL |
Strength Number | 50 |
Strength Unit | mg/g |
Pharmaceutical Classes |