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
76420-634-90	76420-634	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-634-90)
76420-636-01	76420-636	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-01)
76420-636-30	76420-636	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-30)
76420-636-90	76420-636	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-90)
76420-633-30	76420-633	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-30)
76420-633-60	76420-633	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-60)
76420-633-90	76420-633	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA208706	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-90)