Home
>
National Drug Code (NDC)
>
Nizoral
Nizoral - 50458-680-08 - (ketoconazole)
Drug Information of Nizoral
| Product NDC: | 50458-680 |
| Proprietary Name: | Nizoral |
| 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) |
Labeler Information of Nizoral
| Product NDC: | 50458-680 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019927 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900831 |
Package Information of Nizoral
| Package NDC: | 50458-680-08 |
| Package Description: | 120 mL in 1 BOTTLE (50458-680-08) |
NDC Information of Nizoral
| NDC Code | 50458-680-08 |
| Proprietary Name | Nizoral |
| Package Description | 120 mL in 1 BOTTLE (50458-680-08) |
| Product NDC | 50458-680 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketoconazole |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 19900831 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | KETOCONAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
