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Fluconazole - 59762-5029-1 - (fluconazole)

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Drug Information of Fluconazole

Product NDC: 59762-5029
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: 59762-5029
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020090
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19931223

Package Information of Fluconazole

Package NDC: 59762-5029-1
Package Description: 35 mL in 1 BOTTLE (59762-5029-1)

NDC Information of Fluconazole

NDC Code 59762-5029-1
Proprietary Name Fluconazole
Package Description 35 mL in 1 BOTTLE (59762-5029-1)
Product NDC 59762-5029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluconazole
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19931223
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name FLUCONAZOLE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information