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
50228-421-01	50228-421	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50228-421-01)
50228-421-10	50228-421	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (50228-421-10)
50228-421-30	50228-421	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50228-421-30)
50228-420-01	50228-420	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50228-420-01)
50228-420-10	50228-420	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (50228-420-10)
50228-420-30	50228-420	HUMAN PRESCRIPTION DRUG	Fluoxetine	Fluoxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA210935	ScieGen Pharmaceuticals, Inc	FLUOXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50228-420-30)