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
71335-2017-1	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1)
71335-2017-2	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2)
71335-2017-3	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3)
71335-2017-4	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4)
71335-2017-5	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5)
71335-2017-6	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-6)
71335-2017-7	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-7)
71335-2017-8	71335-2017	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220210	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8)
71205-602-30	71205-602	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210820	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30)
71205-602-60	71205-602	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210820	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60)
71205-602-90	71205-602	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210820	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)
68001-595-05	68001-595	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231110	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-05)
68001-595-08	68001-595	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230728	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-08)
68001-595-04	68001-595	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240222	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-04)
71205-358-30	71205-358	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20191114	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-30)
71205-358-60	71205-358	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20191114	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-60)
71205-358-90	71205-358	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20191114	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-90)
70518-2630-0	70518-2630	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200316	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-0)
70518-2630-2	70518-2630	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200728	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-2)
70518-2630-3	70518-2630	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20251009	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-3)