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Fluconazole - 0703-1010-09 - (Fluconazole)

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Drug Information of Fluconazole

Product NDC: 0703-1010
Proprietary Name: Fluconazole
Non Proprietary Name: Fluconazole
Active Ingredient(s): 2    mg/mL & nbsp;   Fluconazole
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 0703-1010
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076653
Marketing Category: ANDA
Start Marketing Date: 20040805

Package Information of Fluconazole

Package NDC: 0703-1010-09
Package Description: 6 VIAL, SINGLE-DOSE in 1 CARTON (0703-1010-09) > 200 mL in 1 VIAL, SINGLE-DOSE (0703-1010-01)

NDC Information of Fluconazole

NDC Code 0703-1010-09
Proprietary Name Fluconazole
Package Description 6 VIAL, SINGLE-DOSE in 1 CARTON (0703-1010-09) > 200 mL in 1 VIAL, SINGLE-DOSE (0703-1010-01)
Product NDC 0703-1010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluconazole
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20040805
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name FLUCONAZOLE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


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