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voriconazole - 0781-5667-13 - (voriconazole)

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Drug Information of voriconazole

Product NDC: 0781-5667
Proprietary Name: voriconazole
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 voriconazole

Product NDC: 0781-5667
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: 0781-5667-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)

NDC Information of voriconazole

NDC Code 0781-5667-13
Proprietary Name voriconazole
Package Description 10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)
Product NDC 0781-5667
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 50
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of voriconazole


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