VFEND - 0049-3170-30 - (VORICONAZOLE)

Alphabetical Index


Drug Information of VFEND

Product NDC: 0049-3170
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)

Labeler Information of VFEND

Product NDC: 0049-3170
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021266
Marketing Category: NDA
Start Marketing Date: 20030328

Package Information of VFEND

Package NDC: 0049-3170-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0049-3170-30)

NDC Information of VFEND

NDC Code 0049-3170-30
Proprietary Name VFEND
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0049-3170-30)
Product NDC 0049-3170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VORICONAZOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030328
Marketing Category Name NDA
Labeler Name Roerig
Substance Name VORICONAZOLE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of VFEND


General Information