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SPORANOX
SPORANOX - 63629-1647-1 - (ITRACONAZOLE)
Drug Information of SPORANOX
| Product NDC: | 63629-1647 |
| Proprietary Name: | SPORANOX |
| Non Proprietary Name: | ITRACONAZOLE |
| Active Ingredient(s): | 100 mg/1 & nbsp; ITRACONAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPORANOX
| Product NDC: | 63629-1647 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020083 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920911 |
Package Information of SPORANOX
| Package NDC: | 63629-1647-1 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (63629-1647-1) |
NDC Information of SPORANOX
| NDC Code | 63629-1647-1 |
| Proprietary Name | SPORANOX |
| Package Description | 30 CAPSULE in 1 BOTTLE (63629-1647-1) |
| Product NDC | 63629-1647 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ITRACONAZOLE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19920911 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | ITRACONAZOLE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
