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
27241-164-30	27241-164	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20190325	N/A	ANDA	ANDA208706	Ajanta Pharma USA Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-164-30)
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)
70518-3287-0	70518-3287	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211209	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-0)
70518-3287-1	70518-3287	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240628	N/A	ANDA	ANDA208706	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-3287-1)
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)
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)
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)
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)
71335-0402-5	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20181112	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-5)
71335-0402-6	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20211227	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-6)
71335-0402-3	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20180411	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-3)
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)
71335-0402-4	71335-0402	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20181030	N/A	ANDA	ANDA208706	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-4)
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)
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)
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)