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Fluconazole - 59762-5015-1 - (fluconazole)

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Drug Information of Fluconazole

Product NDC: 59762-5015
Proprietary Name: Fluconazole
Non Proprietary Name: fluconazole
Active Ingredient(s): 50    mg/1 & nbsp;   fluconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 59762-5015
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019949
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19900129

Package Information of Fluconazole

Package NDC: 59762-5015-1
Package Description: 30 TABLET in 1 BOTTLE (59762-5015-1)

NDC Information of Fluconazole

NDC Code 59762-5015-1
Proprietary Name Fluconazole
Package Description 30 TABLET in 1 BOTTLE (59762-5015-1)
Product NDC 59762-5015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900129
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name FLUCONAZOLE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information