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Mens rogaine
Mens rogaine - 42002-106-13 - (Minoxidil)
Drug Information of Mens rogaine
| 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) |
Labeler Information of Mens rogaine
| 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 Information of Mens rogaine
| Package NDC: | 42002-106-13 |
| Package Description: | 3 CAN in 1 PACKAGE (42002-106-13) > 60 g in 1 CAN |
NDC Information of Mens rogaine
| NDC Code | 42002-106-13 |
| Proprietary Name | Mens rogaine |
| Package Description | 3 CAN in 1 PACKAGE (42002-106-13) > 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 |
