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
71335-1672-6	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210107	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-6)
71335-1672-7	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20210201	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-7)
71335-1672-3	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240404	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-3)
71335-1672-4	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240404	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-4)
71335-1672-1	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20200727	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-1)
71335-1672-8	71335-1672	HUMAN PRESCRIPTION DRUG	Duloxetine	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240404	N/A	ANDA	ANDA203197	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	30 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-8)