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Fluconazole - 54868-5129-1 - (fluconazole)

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Drug Information of Fluconazole

Product NDC: 54868-5129
Proprietary Name: Fluconazole
Non Proprietary Name: fluconazole
Active Ingredient(s): 150    mg/1 & nbsp;   fluconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 54868-5129
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019949
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20040812

Package Information of Fluconazole

Package NDC: 54868-5129-1
Package Description: 12 TABLET in 1 BOTTLE (54868-5129-1)

NDC Information of Fluconazole

NDC Code 54868-5129-1
Proprietary Name Fluconazole
Package Description 12 TABLET in 1 BOTTLE (54868-5129-1)
Product NDC 54868-5129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040812
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name FLUCONAZOLE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information