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
50228-422-10	50228-422	HUMAN PRESCRIPTION DRUG	Fluoxetine	FLUOXETINE HYDROCHLORIDE	TABLET	ORAL	20190110	N/A	ANDA	ANDA211282	ScieGen Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	60 mg/1	1000 TABLET in 1 BOTTLE (50228-422-10)
50228-422-30	50228-422	HUMAN PRESCRIPTION DRUG	Fluoxetine	FLUOXETINE HYDROCHLORIDE	TABLET	ORAL	20190110	N/A	ANDA	ANDA211282	ScieGen Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE (50228-422-30)
50228-638-10	50228-638	HUMAN PRESCRIPTION DRUG	Fluoxetine	FLUOXETINE HYDROCHLORIDE	TABLET	ORAL	20250911	N/A	ANDA	ANDA211282	ScieGen Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	60 mg/1	1000 TABLET in 1 BOTTLE (50228-638-10)
50228-638-30	50228-638	HUMAN PRESCRIPTION DRUG	Fluoxetine	FLUOXETINE HYDROCHLORIDE	TABLET	ORAL	20250911	N/A	ANDA	ANDA211282	ScieGen Pharmaceuticals, Inc.	FLUOXETINE HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE (50228-638-30)