Product NDC: | 55154-2730 |
Proprietary Name: | VFEND |
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) |
Product NDC: | 55154-2730 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021266 |
Marketing Category: | NDA |
Start Marketing Date: | 20020524 |
Package NDC: | 55154-2730-4 |
Package Description: | 30 POUCH in 1 CARTON (55154-2730-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-2730-6) |
NDC Code | 55154-2730-4 |
Proprietary Name | VFEND |
Package Description | 30 POUCH in 1 CARTON (55154-2730-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-2730-6) |
Product NDC | 55154-2730 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | voriconazole |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20020524 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | VORICONAZOLE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |