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
68382-218-02	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	2000 CAPSULE in 1 BOTTLE (68382-218-02)
68382-218-06	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BOTTLE (68382-218-06)
68382-218-10	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	1000 CAPSULE in 1 BOTTLE (68382-218-10)
68382-218-14	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	60 CAPSULE in 1 BOTTLE (68382-218-14)
68382-218-16	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE in 1 BOTTLE (68382-218-16)
68382-218-77	68382-218	HUMAN PRESCRIPTION DRUG	atomoxetine	atomoxetine	CAPSULE	ORAL	20170612	N/A	ANDA	ANDA079017	Zydus Pharmaceuticals USA Inc.	ATOMOXETINE HYDROCHLORIDE	40 mg/1	10 BLISTER PACK in 1 CARTON (68382-218-77) / 10 CAPSULE in 1 BLISTER PACK (68382-218-30)