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
42571-388-01	42571-388	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE in 1 BOTTLE (42571-388-01)
42571-388-10	42571-388	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE in 1 BOTTLE (42571-388-10)
42571-388-30	42571-388	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE in 1 BOTTLE (42571-388-30)
42571-389-01	42571-389	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	40 mg/1	100 CAPSULE in 1 BOTTLE (42571-389-01)
42571-389-10	42571-389	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	40 mg/1	1000 CAPSULE in 1 BOTTLE (42571-389-10)
42571-389-30	42571-389	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (42571-389-30)
42571-387-30	42571-387	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 CAPSULE in 1 BOTTLE (42571-387-30)
42571-387-10	42571-387	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	1000 CAPSULE in 1 BOTTLE (42571-387-10)
42571-387-01	42571-387	HUMAN PRESCRIPTION DRUG	FLUOXETINE	FLUOXETINE	CAPSULE	ORAL	20230101	N/A	ANDA	ANDA216232	Micro Labs Limited	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 CAPSULE in 1 BOTTLE (42571-387-01)