Product NDC: | 43538-530 |
Proprietary Name: | Ketodan |
Non Proprietary Name: | ketoconazole |
Active Ingredient(s): | 20 mg/g & nbsp; ketoconazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43538-530 |
Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091550 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120615 |
Package NDC: | 43538-530-10 |
Package Description: | 1 CAN in 1 CARTON (43538-530-10) > 100 g in 1 CAN |
NDC Code | 43538-530-10 |
Proprietary Name | Ketodan |
Package Description | 1 CAN in 1 CARTON (43538-530-10) > 100 g in 1 CAN |
Product NDC | 43538-530 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ketoconazole |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20120615 |
Marketing Category Name | ANDA |
Labeler Name | Medimetriks Pharmaceuticals, Inc. |
Substance Name | KETOCONAZOLE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |