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
45865-813-30	45865-813	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20150922	N/A	ANDA	ANDA090723	Medsource Pharmaceuticals	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (45865-813-30)
45865-813-60	45865-813	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20150922	N/A	ANDA	ANDA090723	Medsource Pharmaceuticals	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (45865-813-60)
25000-610-03	25000-610	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220527	N/A	ANDA	ANDA090723	MARKSANS PHARMA LIMITED	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-610-03)
25000-610-07	25000-610	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220527	N/A	ANDA	ANDA090723	MARKSANS PHARMA LIMITED	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-610-07)
25000-609-07	25000-609	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220527	N/A	ANDA	ANDA090723	MARKSANS PHARMA LIMITED	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-07)
25000-609-03	25000-609	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220527	N/A	ANDA	ANDA090723	MARKSANS PHARMA LIMITED	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-03)
25000-608-06	25000-608	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20220527	N/A	ANDA	ANDA090723	MARKSANS PHARMA LIMITED	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-608-06)