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Fluconazole - 65862-059-01 - (Fluconazole)

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Drug Information of Fluconazole

Product NDC: 65862-059
Proprietary Name: Fluconazole
Non Proprietary Name: Fluconazole
Active Ingredient(s): 100    mg/1 & nbsp;   Fluconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 65862-059
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077731
Marketing Category: ANDA
Start Marketing Date: 20081007

Package Information of Fluconazole

Package NDC: 65862-059-01
Package Description: 100 TABLET in 1 BOTTLE (65862-059-01)

NDC Information of Fluconazole

NDC Code 65862-059-01
Proprietary Name Fluconazole
Package Description 100 TABLET in 1 BOTTLE (65862-059-01)
Product NDC 65862-059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081007
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name FLUCONAZOLE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


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