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itraconazole
itraconazole - 0185-0550-01 - (itraconazole)
Drug Information of itraconazole
| Product NDC: | 0185-0550 |
| Proprietary Name: | itraconazole |
| 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 itraconazole
| Product NDC: | 0185-0550 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076105 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040528 |
Package Information of itraconazole
| Package NDC: | 0185-0550-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0185-0550-01) |
NDC Information of itraconazole
| NDC Code | 0185-0550-01 |
| Proprietary Name | itraconazole |
| Package Description | 100 CAPSULE in 1 BOTTLE (0185-0550-01) |
| Product NDC | 0185-0550 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | itraconazole |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20040528 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | ITRACONAZOLE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
