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Womens Rogaine
Womens Rogaine - 42002-105-02 - (Minoxidil)
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: | 42002-105-02 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (42002-105-02) > 60 mL in 1 BOTTLE, PLASTIC |
NDC Information of Womens Rogaine
| NDC Code | 42002-105-02 |
| Proprietary Name | Womens Rogaine |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (42002-105-02) > 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 |
