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Fluconazole - 54868-5248-0 - (fluconazole)

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Drug Information of Fluconazole

Product NDC: 54868-5248
Proprietary Name: Fluconazole
Non Proprietary Name: fluconazole
Active Ingredient(s): 10    mg/mL & nbsp;   fluconazole
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 54868-5248
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020090
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20050311

Package Information of Fluconazole

Package NDC: 54868-5248-0
Package Description: 1 BOTTLE in 1 CARTON (54868-5248-0) > 35 mL in 1 BOTTLE

NDC Information of Fluconazole

NDC Code 54868-5248-0
Proprietary Name Fluconazole
Package Description 1 BOTTLE in 1 CARTON (54868-5248-0) > 35 mL in 1 BOTTLE
Product NDC 54868-5248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluconazole
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20050311
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name FLUCONAZOLE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information