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
71335-2537-5	71335-2537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241210	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-5)
68071-3775-9	68071-3775	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250120	N/A	ANDA	ANDA090694	NuCare Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3775-9)
50090-7784-0	50090-7784	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20251121	N/A	ANDA	ANDA090694	A-S Medication Solutions	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7784-0)
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)
68180-296-09	68180-296	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140626	N/A	ANDA	ANDA090694	Lupin Pharmaceuticals, Inc.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-09)
67046-1585-3	67046-1585	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20250915	N/A	ANDA	ANDA090694	Coupler LLC	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1585-3)
71335-2537-6	71335-2537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241210	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-6)
71335-2537-7	71335-2537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241210	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-7)
71335-2537-8	71335-2537	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20241210	N/A	ANDA	ANDA090694	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-8)
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)