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
63187-089-30	63187-089	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20181101	N/A	ANDA	ANDA076990	Proficient Rx LP	FLUOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (63187-089-30)
63187-089-90	63187-089	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20181101	N/A	ANDA	ANDA076990	Proficient Rx LP	FLUOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE in 1 BOTTLE (63187-089-90)
63304-632-01	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	100 CAPSULE in 1 BOTTLE (63304-632-01)
63304-632-05	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	500 CAPSULE in 1 BOTTLE (63304-632-05)
63304-632-10	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	1000 CAPSULE in 1 BOTTLE (63304-632-10)
63304-632-30	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (63304-632-30)
63304-632-80	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	100 BLISTER PACK in 1 CARTON (63304-632-80) / 1 CAPSULE in 1 BLISTER PACK
63304-632-90	63304-632	HUMAN PRESCRIPTION DRUG	Fluoxetine	fluoxetine	CAPSULE	ORAL	20180816	N/A	ANDA	ANDA076990	Sun Pharmaceutical Industries, Inc.	FLUOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE in 1 BOTTLE (63304-632-90)