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voriconazole
voriconazole - 0781-5667-13 - (voriconazole)
Drug Information of voriconazole
| Product NDC: | 0781-5667 |
| Proprietary Name: | voriconazole |
| Non Proprietary Name: | voriconazole |
| Active Ingredient(s): | 50 mg/1 & nbsp; voriconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of voriconazole
| Product NDC: | 0781-5667 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200265 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111212 |
Package Information of voriconazole
| Package NDC: | 0781-5667-13 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06) |
NDC Information of voriconazole
| NDC Code | 0781-5667-13 |
| Proprietary Name | voriconazole |
| Package Description | 10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06) |
| Product NDC | 0781-5667 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | voriconazole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111212 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | VORICONAZOLE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
