Product NDC: | 68788-9903 |
Proprietary Name: | Ketoconazole |
Non Proprietary Name: | Ketoconazole |
Active Ingredient(s): | 20 mg/mL & nbsp; Ketoconazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO, SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9903 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076419 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120130 |
Package NDC: | 68788-9903-1 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (68788-9903-1) |
NDC Code | 68788-9903-1 |
Proprietary Name | Ketoconazole |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (68788-9903-1) |
Product NDC | 68788-9903 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ketoconazole |
Dosage Form Name | SHAMPOO, SUSPENSION |
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/mL |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |