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KETOCONAZOLE
KETOCONAZOLE - 0179-0055-70 - (KETOCONAZOLE)
Drug Information of KETOCONAZOLE
| Product NDC: | 0179-0055 |
| Proprietary Name: | KETOCONAZOLE |
| Non Proprietary Name: | KETOCONAZOLE |
| Active Ingredient(s): | 200 mg/1 & nbsp; KETOCONAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KETOCONAZOLE
| Product NDC: | 0179-0055 |
| Labeler Name: | KAISER FOUNDATION HOSPITALS |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075597 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100302 |
Package Information of KETOCONAZOLE
| Package NDC: | 0179-0055-70 |
| Package Description: | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0055-70) |
NDC Information of KETOCONAZOLE
| NDC Code | 0179-0055-70 |
| Proprietary Name | KETOCONAZOLE |
| Package Description | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0055-70) |
| Product NDC | 0179-0055 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | KETOCONAZOLE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100302 |
| Marketing Category Name | ANDA |
| Labeler Name | KAISER FOUNDATION HOSPITALS |
| Substance Name | KETOCONAZOLE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
