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Voriconazole
Voriconazole - 0781-3416-94 - (Voriconazole)
Drug Information of Voriconazole
| Product NDC: | 0781-3416 |
| Proprietary Name: | Voriconazole |
| Non Proprietary Name: | Voriconazole |
| Active Ingredient(s): | 10 mg/mL & nbsp; Voriconazole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Voriconazole
| Product NDC: | 0781-3416 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090862 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120530 |
Package Information of Voriconazole
| Package NDC: | 0781-3416-94 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0781-3416-94) > 20 mL in 1 VIAL, SINGLE-USE |
NDC Information of Voriconazole
| NDC Code | 0781-3416-94 |
| Proprietary Name | Voriconazole |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0781-3416-94) > 20 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0781-3416 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Voriconazole |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120530 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | VORICONAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
