Product NDC: | 0363-0856 |
Proprietary Name: | 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) |
Product NDC: | 0363-0856 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075357 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060914 |
Package NDC: | 0363-0856-30 |
Package Description: | 3 BOTTLE in 1 CARTON (0363-0856-30) > 60 mL in 1 BOTTLE |
NDC Code | 0363-0856-30 |
Proprietary Name | Minoxidil |
Package Description | 3 BOTTLE in 1 CARTON (0363-0856-30) > 60 mL in 1 BOTTLE |
Product NDC | 0363-0856 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Minoxidil |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20060914 |
Marketing Category Name | ANDA |
Labeler Name | Walgreen Company |
Substance Name | MINOXIDIL |
Strength Number | 2 |
Strength Unit | g/100mL |
Pharmaceutical Classes |