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
72241-007-22	72241-007	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20210908	N/A	ANDA	ANDA206993	Modavar Pharmaceuticals LLC	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 CAPSULE in 1 BOTTLE (72241-007-22)
71209-041-01	71209-041	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20221215	N/A	ANDA	ANDA206993	Cadila Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE in 1 BOTTLE (71209-041-01)
71209-041-05	71209-041	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20221215	N/A	ANDA	ANDA206993	Cadila Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE in 1 BOTTLE (71209-041-05)
71209-041-10	71209-041	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20221215	N/A	ANDA	ANDA206993	Cadila Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE in 1 BOTTLE (71209-041-10)
71209-041-11	71209-041	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	CAPSULE	ORAL	20221215	N/A	ANDA	ANDA206993	Cadila Pharmaceuticals Limited	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE in 1 BOTTLE (71209-041-11)