VFEND - 0049-3190-01 - (VORICONAZOLE)

Alphabetical Index


Drug Information of VFEND

Product NDC: 0049-3190
Proprietary Name: VFEND
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 VFEND

Product NDC: 0049-3190
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021267
Marketing Category: NDA
Start Marketing Date: 20030328

Package Information of VFEND

Package NDC: 0049-3190-01
Package Description: 20 mL in 1 VIAL, SINGLE-USE (0049-3190-01)

NDC Information of VFEND

NDC Code 0049-3190-01
Proprietary Name VFEND
Package Description 20 mL in 1 VIAL, SINGLE-USE (0049-3190-01)
Product NDC 0049-3190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VORICONAZOLE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030328
Marketing Category Name NDA
Labeler Name Roerig
Substance Name VORICONAZOLE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of VFEND


General Information