Product NDC: | 68084-205 |
Proprietary Name: | Minoxidil |
Non Proprietary Name: | Minoxidil |
Active Ingredient(s): | 10 mg/1 & nbsp; Minoxidil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68084-205 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071839 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070730 |
Package NDC: | 68084-205-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (68084-205-01) > 10 TABLET in 1 BLISTER PACK (68084-205-11) |
NDC Code | 68084-205-01 |
Proprietary Name | Minoxidil |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-205-01) > 10 TABLET in 1 BLISTER PACK (68084-205-11) |
Product NDC | 68084-205 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Minoxidil |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070730 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | MINOXIDIL |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |