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
71335-0402-1	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180302	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-1)
71335-0402-2	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211227	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-2)
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)
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)
27241-098-10	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	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-10)
68788-7672-0	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-0)
68788-7672-1	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-1)
68788-7672-2	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-2)
68788-7672-3	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-3)
68788-7672-6	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-6)
68788-7672-8	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-8)
68788-7672-9	68788-7672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200228	N/A	ANDA	ANDA208706	Preferred Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-9)
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)
71205-005-30	71205-005	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180402	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-30)
71205-005-60	71205-005	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180402	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-60)
71205-005-90	71205-005	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180402	N/A	ANDA	ANDA208706	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-90)
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)