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
68180-998-01	68180-998	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20190807	N/A	ANDA	ANDA211653	Lupin Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (68180-998-01)
68180-998-06	68180-998	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20190807	N/A	ANDA	ANDA211653	Lupin Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (68180-998-06)
53002-1796-0	53002-1796	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20221231	N/A	ANDA	ANDA211653	RPK Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (53002-1796-0)
53002-1796-3	53002-1796	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20221231	N/A	ANDA	ANDA211653	RPK Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (53002-1796-3)
68180-999-01	68180-999	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20190807	N/A	ANDA	ANDA211653	Lupin Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (68180-999-01)
68180-999-06	68180-999	HUMAN PRESCRIPTION DRUG	Fluoxetine Hydrochloride	Fluoxetine Hydrochloride	TABLET	ORAL	20190807	N/A	ANDA	ANDA211653	Lupin Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (68180-999-06)