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
82804-024-90	82804-024	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20231016	N/A	ANDA	ANDA203088	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90)
72162-1598-9	72162-1598	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240205	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1598-9)
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)
68788-8362-3	68788-8362	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20230201	N/A	ANDA	ANDA203088	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)
68788-8362-9	68788-8362	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20230201	N/A	ANDA	ANDA203088	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9)