| 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] |