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Ketoconazole
Ketoconazole - 49349-379-02 - (Ketoconazole)
Drug Information of Ketoconazole
| Product NDC: | 49349-379 |
| 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: | 49349-379 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075597 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110714 |
Package Information of Ketoconazole
| Package NDC: | 49349-379-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-379-02) |
NDC Information of Ketoconazole
| NDC Code | 49349-379-02 |
| Proprietary Name | Ketoconazole |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-379-02) |
| Product NDC | 49349-379 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketoconazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110714 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | KETOCONAZOLE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
