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
16714-758-01	16714-758	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20180601	N/A	ANDA	ANDA079019	Northstar Rx LLC	ATOMOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (16714-758-01)
16714-759-01	16714-759	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20180601	N/A	ANDA	ANDA079019	Northstar Rx LLC	ATOMOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE in 1 BOTTLE (16714-759-01)
16714-760-01	16714-760	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20180601	N/A	ANDA	ANDA079019	Northstar Rx LLC	ATOMOXETINE HYDROCHLORIDE	80 mg/1	30 CAPSULE in 1 BOTTLE (16714-760-01)
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)
68462-269-30	68462-269	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE in 1 BOTTLE (68462-269-30)
68462-270-23	68462-270	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170530	N/A	ANDA	ANDA079019	Glenmark Pharmaceuticals Inc., USA	ATOMOXETINE HYDROCHLORIDE	80 mg/1	2000 CAPSULE in 1 BOTTLE (68462-270-23)
50090-7342-0	50090-7342	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20241016	N/A	ANDA	ANDA079019	A-S Medication Solutions	ATOMOXETINE HYDROCHLORIDE	25 mg/1	30 CAPSULE in 1 BOTTLE (50090-7342-0)