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
76420-236-30	76420-236	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20220707	N/A	ANDA	ANDA090776	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-30)
76420-236-60	76420-236	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20220707	N/A	ANDA	ANDA090776	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-60)
76420-236-90	76420-236	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20220707	N/A	ANDA	ANDA090776	Asclemed USA, Inc.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-90)