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
51655-237-25	51655-237	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210423	N/A	ANDA	ANDA208706	Northwind Pharmaceuticals	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)
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)
53002-1494-3	53002-1494	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170901	N/A	ANDA	ANDA208706	RPK Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53002-1494-3)
53002-1503-3	53002-1503	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220101	N/A	ANDA	ANDA208706	RPK Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53002-1503-3)
80425-0119-1	80425-0119	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-1)
80425-0119-2	80425-0119	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-2)
80425-0119-3	80425-0119	HUMAN PRESCRIPTION DRUG	Duloxetine DR	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230330	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-3)
53002-1561-3	53002-1561	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170901	N/A	ANDA	ANDA208706	RPK Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53002-1561-3)
80425-0146-1	80425-0146	HUMAN PRESCRIPTION DRUG	Duloxetine HCL DR	Duloxetine HCL	CAPSULE, DELAYED RELEASE	ORAL	20230614	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-1)
80425-0146-2	80425-0146	HUMAN PRESCRIPTION DRUG	Duloxetine HCL DR	Duloxetine HCL	CAPSULE, DELAYED RELEASE	ORAL	20230614	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-2)
80425-0146-3	80425-0146	HUMAN PRESCRIPTION DRUG	Duloxetine HCL DR	Duloxetine HCL	CAPSULE, DELAYED RELEASE	ORAL	20230614	N/A	ANDA	ANDA208706	Advanced Rx Pharmacy of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-3)
55700-605-30	55700-605	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180420	N/A	ANDA	ANDA208706	Quality Care Products LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-30)
55700-605-60	55700-605	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180420	N/A	ANDA	ANDA208706	Quality Care Products LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-60)