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
60760-759-30	60760-759	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250715	N/A	ANDA	ANDA208706	ST. MARY'S MEDICAL PARK PHARMACY	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-759-30)
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)
72189-661-60	72189-661	HUMAN PRESCRIPTION DRUG	Duloxetine D/R	Duloxetine D/R	CAPSULE, DELAYED RELEASE	ORAL	20260209	N/A	ANDA	ANDA208706	Direct_Rx	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-60)
50090-6893-0	50090-6893	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231207	N/A	ANDA	ANDA208706	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6893-0)
72189-661-30	72189-661	HUMAN PRESCRIPTION DRUG	Duloxetine D/R	Duloxetine D/R	CAPSULE, DELAYED RELEASE	ORAL	20260209	N/A	ANDA	ANDA208706	Direct_Rx	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-30)
68071-3766-9	68071-3766	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250110	N/A	ANDA	ANDA208706	NuCare Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)
68071-3519-3	68071-3519	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231010	N/A	ANDA	ANDA208706	NuCare Pharmaceuticals,Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3519-3)
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)
71335-2017-5	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)
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)
71335-2017-4	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)