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Voriconazole - 51079-165-03 - (voriconazole)

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Drug Information of Voriconazole

Product NDC: 51079-165
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: 51079-165
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090547
Marketing Category: ANDA
Start Marketing Date: 20120921

Package Information of Voriconazole

Package NDC: 51079-165-03
Package Description: 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-165-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-165-01)

NDC Information of Voriconazole

NDC Code 51079-165-03
Proprietary Name Voriconazole
Package Description 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-165-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-165-01)
Product NDC 51079-165
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name voriconazole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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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