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Voriconazole - 0378-1640-93 - (voriconazole)

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Drug Information of Voriconazole

Product NDC: 0378-1640
Proprietary Name: Voriconazole
Non Proprietary Name: voriconazole
Active Ingredient(s): 200    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: 0378-1640
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090547
Marketing Category: ANDA
Start Marketing Date: 20120131

Package Information of Voriconazole

Package NDC: 0378-1640-93
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1640-93)

NDC Information of Voriconazole

NDC Code 0378-1640-93
Proprietary Name Voriconazole
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1640-93)
Product NDC 0378-1640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name voriconazole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120131
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name VORICONAZOLE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Voriconazole


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