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Fluconazole - 0703-1029-30 - (Fluconazole)

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Drug Information of Fluconazole

Product NDC: 0703-1029
Proprietary Name: Fluconazole
Non Proprietary Name: Fluconazole
Active Ingredient(s): 200    mg/100mL & nbsp;   Fluconazole
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 0703-1029
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076837
Marketing Category: ANDA
Start Marketing Date: 20050316

Package Information of Fluconazole

Package NDC: 0703-1029-30
Package Description: 6 BAG in 1 CARTON (0703-1029-30) > 100 mL in 1 BAG (0703-1029-31)

NDC Information of Fluconazole

NDC Code 0703-1029-30
Proprietary Name Fluconazole
Package Description 6 BAG in 1 CARTON (0703-1029-30) > 100 mL in 1 BAG (0703-1029-31)
Product NDC 0703-1029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluconazole
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20050316
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name FLUCONAZOLE
Strength Number 200
Strength Unit mg/100mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


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