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Fluconazole - 59762-5035-2 - (fluconazole)

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Drug Information of Fluconazole

Product NDC: 59762-5035
Proprietary Name: Fluconazole
Non Proprietary Name: fluconazole
Active Ingredient(s): 2    mg/mL & nbsp;   fluconazole
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 59762-5035
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019950
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19900129

Package Information of Fluconazole

Package NDC: 59762-5035-2
Package Description: 6 CONTAINER in 1 CARTON (59762-5035-2) > 200 mL in 1 CONTAINER

NDC Information of Fluconazole

NDC Code 59762-5035-2
Proprietary Name Fluconazole
Package Description 6 CONTAINER in 1 CARTON (59762-5035-2) > 200 mL in 1 CONTAINER
Product NDC 59762-5035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluconazole
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19900129
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name FLUCONAZOLE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information