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ketoconazole
ketoconazole - 52125-495-01 - (ketoconazole)
Drug Information of ketoconazole
| Product NDC: | 52125-495 |
| Proprietary Name: | ketoconazole |
| Non Proprietary Name: | ketoconazole |
| Active Ingredient(s): | 20 mg/1 & nbsp; ketoconazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ketoconazole
| Product NDC: | 52125-495 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076294 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130415 |
Package Information of ketoconazole
| Package NDC: | 52125-495-01 |
| Package Description: | 1 CREAM in 1 CARTON (52125-495-01) |
NDC Information of ketoconazole
| NDC Code | 52125-495-01 |
| Proprietary Name | ketoconazole |
| Package Description | 1 CREAM in 1 CARTON (52125-495-01) |
| Product NDC | 52125-495 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketoconazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130415 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | KETOCONAZOLE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
