"57237-004-30" National Drug Code (NDC)

NDC Code	57237-004-30
Package Description	30 TABLET in 1 BOTTLE (57237-004-30)
Product NDC	57237-004
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fluconazole
Non-Proprietary Name	Fluconazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20081007
Marketing Category Name	ANDA
Application Number	ANDA077731
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	FLUCONAZOLE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]