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
63629-2063-1	63629-2063	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-2063-1)
71335-0165-1	71335-0165	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180503	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1)
71335-0165-2	71335-0165	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180712	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-2)
71335-0165-3	71335-0165	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20211227	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-3)
71335-0165-4	71335-0165	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180524	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-4)
51991-747-10	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)
51991-747-33	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-33)
51991-747-90	51991-747	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20140611	N/A	ANDA	ANDA203088	Breckenridge Pharmaceutical, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-90)
68001-368-04	68001-368	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	BluePoint Laboratories	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68001-368-04)
71610-743-30	71610-743	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-30)
71610-743-53	71610-743	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-53)
71610-743-60	71610-743	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-60)
71610-743-74	71610-743	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20250605	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-74)
71610-743-80	71610-743	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240320	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-80)
72162-1600-3	72162-1600	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20180521	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1600-3)
82009-031-90	82009-031	HUMAN PRESCRIPTION DRUG	Duloxetine	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20230601	N/A	ANDA	ANDA203088	Quallent Pharmaceuticals Health, LLC	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-031-90)
68788-7897-3	68788-7897	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20210514	N/A	ANDA	ANDA203088	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-3)
71610-739-16	71610-739	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240108	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	6000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-16)
71610-739-33	71610-739	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240322	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	840 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-33)
71610-739-74	71610-739	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20230927	N/A	ANDA	ANDA203088	Aphena Pharma Solutions - Tennessee, LLC	DULOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-74)