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Ketoconazole
Ketoconazole - 68788-9915-3 - (Ketoconazole)
Drug Information of Ketoconazole
| Product NDC: | 68788-9915 |
| Proprietary Name: | Ketoconazole |
| Non Proprietary Name: | Ketoconazole |
| Active Ingredient(s): | 20 mg/g & nbsp; Ketoconazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketoconazole
| Product NDC: | 68788-9915 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075638 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120130 |
Package Information of Ketoconazole
| Package NDC: | 68788-9915-3 |
| Package Description: | 1 TUBE in 1 CARTON (68788-9915-3) > 30 g in 1 TUBE |
NDC Information of Ketoconazole
| NDC Code | 68788-9915-3 |
| Proprietary Name | Ketoconazole |
| Package Description | 1 TUBE in 1 CARTON (68788-9915-3) > 30 g in 1 TUBE |
| Product NDC | 68788-9915 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketoconazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120130 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | KETOCONAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
