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
67877-265-10	67877-265	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10)
67877-265-30	67877-265	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-30)
67877-265-90	67877-265	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-90)
67877-263-30	67877-263	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-30)
67877-263-60	67877-263	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-60)
67877-263-01	67877-263	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-263-01)