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
71335-2567-1	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-1)
71335-2567-2	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-2)
71335-2567-3	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-3)
71335-2567-4	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-4)
71335-2567-5	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-5)
71335-2567-6	71335-2567	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250205	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-6)
68180-296-03	68180-296	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090694	Lupin Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-03)
68180-296-06	68180-296	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090694	Lupin Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-06)
80425-0389-1	80425-0389	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240522	N/A	ANDA	ANDA090694	Advanced Rx of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-1)
80425-0389-2	80425-0389	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240522	N/A	ANDA	ANDA090694	Advanced Rx of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-2)
80425-0389-3	80425-0389	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240522	N/A	ANDA	ANDA090694	Advanced Rx of Tennessee, LLC	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-3)
71335-2624-1	71335-2624	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-1)
71335-2624-2	71335-2624	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-2)
71335-2624-3	71335-2624	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-3)
71335-2624-4	71335-2624	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-4)
68180-297-06	68180-297	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20150715	N/A	ANDA	ANDA090694	Lupin Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-297-06)
68788-8782-3	68788-8782	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241211	N/A	ANDA	ANDA090694	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-3)
68788-8782-6	68788-8782	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241211	N/A	ANDA	ANDA090694	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-6)
68788-8782-9	68788-8782	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241211	N/A	ANDA	ANDA090694	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8782-9)
68180-295-03	68180-295	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140306	N/A	ANDA	ANDA090694	Lupin Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-03)