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voriconazole - 0781-5668-05 - (voriconazole)

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Drug Information of voriconazole

Product NDC: 0781-5668
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: 0781-5668
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200265
Marketing Category: ANDA
Start Marketing Date: 20111212

Package Information of voriconazole

Package NDC: 0781-5668-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0781-5668-05)

NDC Information of voriconazole

NDC Code 0781-5668-05
Proprietary Name voriconazole
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0781-5668-05)
Product NDC 0781-5668
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name voriconazole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111212
Marketing Category Name ANDA
Labeler Name Sandoz 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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