"57237-149-35" National Drug Code (NDC)

NDC Code	57237-149-35
Package Description	1 BOTTLE in 1 CARTON (57237-149-35) / 35 mL in 1 BOTTLE
Product NDC	57237-149
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fluconazole
Non-Proprietary Name	Fluconazole
Dosage Form	POWDER, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20090918
Marketing Category Name	ANDA
Application Number	ANDA079150
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	FLUCONAZOLE
Strength	10
Strength Unit	mg/mL
Pharmacy Classes	Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]