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
71335-1048-7	71335-1048	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20240517	N/A	ANDA	ANDA076001	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 CAPSULE in 1 BOTTLE (71335-1048-7)
71335-1048-8	71335-1048	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20240517	N/A	ANDA	ANDA076001	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	10 mg/1	180 CAPSULE in 1 BOTTLE (71335-1048-8)
71335-0924-8	71335-0924	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20220921	N/A	ANDA	ANDA076001	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	20 mg/1	120 CAPSULE in 1 BOTTLE (71335-0924-8)
71335-0924-9	71335-0924	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20220921	N/A	ANDA	ANDA076001	Bryant Ranch Prepack	FLUOXETINE HYDROCHLORIDE	20 mg/1	45 CAPSULE in 1 BOTTLE (71335-0924-9)
0615-7625-05	0615-7625	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20190415	N/A	ANDA	ANDA076001	NCS HealthCare of KY, LLC dba Vangard Labs	FLUOXETINE HYDROCHLORIDE	20 mg/1	15 CAPSULE in 1 BLISTER PACK (0615-7625-05)
0615-7625-39	0615-7625	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20110520	N/A	ANDA	ANDA076001	NCS HealthCare of KY, LLC dba Vangard Labs	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE in 1 BLISTER PACK (0615-7625-39)