Product NDC: | 10147-0750 |
Proprietary Name: | KETOCONAZOLE |
Non Proprietary Name: | ketoconazole |
Active Ingredient(s): | 20 mg/mL & nbsp; ketoconazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10147-0750 |
Labeler Name: | Patriot Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019927 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20050701 |
Package NDC: | 10147-0750-4 |
Package Description: | 120 mL in 1 BOTTLE (10147-0750-4) |
NDC Code | 10147-0750-4 |
Proprietary Name | KETOCONAZOLE |
Package Description | 120 mL in 1 BOTTLE (10147-0750-4) |
Product NDC | 10147-0750 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ketoconazole |
Dosage Form Name | SHAMPOO |
Route Name | TOPICAL |
Start Marketing Date | 20050701 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Patriot Pharmaceuticals, LLC |
Substance Name | KETOCONAZOLE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |