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
16714-757-01	16714-757	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20180601	N/A	ANDA	ANDA079019	Northstar Rx LLC	ATOMOXETINE HYDROCHLORIDE	25 mg/1	30 CAPSULE in 1 BOTTLE (16714-757-01)
16714-761-01	16714-761	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20180601	N/A	ANDA	ANDA079019	Northstar Rx LLC	ATOMOXETINE HYDROCHLORIDE	100 mg/1	30 CAPSULE in 1 BOTTLE (16714-761-01)
68462-267-23	68462-267	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	25 mg/1	2000 CAPSULE in 1 BOTTLE (68462-267-23)
68462-267-30	68462-267	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	25 mg/1	30 CAPSULE in 1 BOTTLE (68462-267-30)
68462-271-30	68462-271	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	100 mg/1	30 CAPSULE in 1 BOTTLE (68462-271-30)
68462-271-51	68462-271	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	100 mg/1	1500 CAPSULE in 1 BOTTLE (68462-271-51)
50090-7397-0	50090-7397	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20241023	N/A	ANDA	ANDA079019	A-S Medication Solutions	ATOMOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE in 1 BOTTLE (50090-7397-0)