美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
57237-150-35	57237-150	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	Rising Pharma Holdings, Inc.	FLUCONAZOLE	40 mg/mL	1 BOTTLE in 1 CARTON (57237-150-35) / 35 mL in 1 BOTTLE
16714-695-01	16714-695	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	NorthStar Rx LLC	FLUCONAZOLE	10 mg/mL	1 BOTTLE in 1 CARTON (16714-695-01) / 35 mL in 1 BOTTLE
16714-696-01	16714-696	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	NorthStar Rx LLC	FLUCONAZOLE	40 mg/mL	1 BOTTLE in 1 CARTON (16714-696-01) / 35 mL in 1 BOTTLE
57237-149-35	57237-149	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	Rising Pharma Holdings, Inc.	FLUCONAZOLE	10 mg/mL	1 BOTTLE in 1 CARTON (57237-149-35) / 35 mL in 1 BOTTLE
65862-300-35	65862-300	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	Aurobindo Pharma Limited	FLUCONAZOLE	40 mg/mL	1 BOTTLE in 1 CARTON (65862-300-35) / 35 mL in 1 BOTTLE
65862-299-35	65862-299	HUMAN PRESCRIPTION DRUG	Fluconazole	Fluconazole	POWDER, FOR SUSPENSION	ORAL	20090918	N/A	ANDA	ANDA079150	Aurobindo Pharma Limited	FLUCONAZOLE	10 mg/mL	1 BOTTLE in 1 CARTON (65862-299-35) / 35 mL in 1 BOTTLE