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Nizoral
Nizoral - 50580-895-07 - (Ketoconazole)
Drug Information of Nizoral
| Product NDC: | 50580-895 |
| Proprietary Name: | Nizoral |
| Non Proprietary Name: | Ketoconazole |
| Active Ingredient(s): | 10 mg/mL & nbsp; Ketoconazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nizoral
| Product NDC: | 50580-895 |
| Labeler Name: | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020310 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990401 |
Package Information of Nizoral
| Package NDC: | 50580-895-07 |
| Package Description: | 1 BOTTLE in 1 CARTON (50580-895-07) > 200 mL in 1 BOTTLE |
NDC Information of Nizoral
| NDC Code | 50580-895-07 |
| Proprietary Name | Nizoral |
| Package Description | 1 BOTTLE in 1 CARTON (50580-895-07) > 200 mL in 1 BOTTLE |
| Product NDC | 50580-895 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ketoconazole |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 19990401 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Substance Name | KETOCONAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
