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
71335-0509-3	71335-0509	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20210224	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-3)
71335-0509-4	71335-0509	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20210407	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-4)
71335-0509-5	71335-0509	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20220831	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-5)
71335-0509-6	71335-0509	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20240529	N/A	ANDA	ANDA203088	Bryant Ranch Prepack	DULOXETINE HYDROCHLORIDE	60 mg/1	120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-6)
70518-0122-5	70518-0122	HUMAN PRESCRIPTION DRUG	Duloxetine Delayed-Release	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE PELLETS	ORAL	20241002	N/A	ANDA	ANDA203088	REMEDYREPACK INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-0122-5)