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Fluconazole - 21695-560-07 - (Fluconazole)

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Drug Information of Fluconazole

Product NDC: 21695-560
Proprietary Name: Fluconazole
Non Proprietary Name: Fluconazole
Active Ingredient(s): 200    mg/1 & nbsp;   Fluconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 21695-560
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077253
Marketing Category: ANDA
Start Marketing Date: 20060125

Package Information of Fluconazole

Package NDC: 21695-560-07
Package Description: 7 TABLET in 1 BOTTLE (21695-560-07)

NDC Information of Fluconazole

NDC Code 21695-560-07
Proprietary Name Fluconazole
Package Description 7 TABLET in 1 BOTTLE (21695-560-07)
Product NDC 21695-560
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060125
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name FLUCONAZOLE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


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