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
72789-338-90	72789-338	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230728	N/A	ANDA	ANDA208706	PD-Rx Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)
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)
27241-097-05	27241-097	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211018	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-05)
27241-097-06	27241-097	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-06)
27241-097-10	27241-097	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-10)
27241-097-90	27241-097	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211018	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-90)
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)
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)
50090-5940-0	50090-5940	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220314	N/A	ANDA	ANDA208706	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5940-0)
50090-5940-1	50090-5940	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20220314	N/A	ANDA	ANDA208706	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5940-1)
27241-099-03	27241-099	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-03)
27241-099-40	27241-099	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211018	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-40)
27241-099-90	27241-099	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-90)
68001-594-06	68001-594	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231111	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-594-06)
51655-237-25	51655-237	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210423	N/A	ANDA	ANDA208706	Northwind Health Company, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)
27241-098-03	27241-098	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-03)
27241-098-09	27241-098	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-09)