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
67877-264-10	67877-264	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-10)
67877-264-30	67877-264	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-30)
67877-264-90	67877-264	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20120501	N/A	ANDA	ANDA203197	Ascend Laboratories, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-90)
71205-445-30	71205-445	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200519	N/A	ANDA	ANDA203197	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-30)
71205-445-60	71205-445	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200519	N/A	ANDA	ANDA203197	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-60)
71205-445-90	71205-445	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200519	N/A	ANDA	ANDA203197	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-90)