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Fluconazole - 49349-729-02 - (Fluconazole)

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Drug Information of Fluconazole

Product NDC: 49349-729
Proprietary Name: Fluconazole
Non Proprietary Name: Fluconazole
Active Ingredient(s): 150    mg/1 & nbsp;   Fluconazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluconazole

Product NDC: 49349-729
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076042
Marketing Category: ANDA
Start Marketing Date: 20110823

Package Information of Fluconazole

Package NDC: 49349-729-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-729-02)

NDC Information of Fluconazole

NDC Code 49349-729-02
Proprietary Name Fluconazole
Package Description 30 TABLET in 1 BLISTER PACK (49349-729-02)
Product NDC 49349-729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluconazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110823
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name FLUCONAZOLE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Fluconazole


General Information