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
70518-1054-0	70518-1054	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180309	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-0)
70518-1054-6	70518-1054	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210609	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-6)
70518-1054-7	70518-1054	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210625	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-7)
70518-1054-9	70518-1054	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211202	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-9)
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)
60760-462-60	60760-462	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250916	N/A	ANDA	ANDA208706	ST. MARY'S MEDICAL PARK PHARMACY	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-462-60)
70518-1011-0	70518-1011	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180212	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1011-0)
70518-1011-1	70518-1011	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20190417	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-1)
70518-1011-2	70518-1011	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200504	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-2)
68001-596-04	68001-596	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230728	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-596-04)
68001-596-08	68001-596	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20230728	N/A	ANDA	ANDA208706	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-596-08)
68788-7935-3	68788-7935	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210615	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-3)
68788-7935-6	68788-7935	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210615	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-6)
68788-7935-9	68788-7935	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210615	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-9)
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)
87448-2201-6	87448-2201	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20170316	N/A	ANDA	ANDA208706	Northwestern Memorial HealthCare	DULOXETINE HYDROCHLORIDE	20 mg/1	1 CAPSULE, DELAYED RELEASE in 1 POUCH (87448-2201-6)
70518-1139-0	70518-1139	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180425	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-0)