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
82804-024-60	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	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60)
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)
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)
68788-8362-0	68788-8362	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20230314	N/A	ANDA	ANDA203088	Preferred Pharmaceuticals Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0)
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)