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
13668-110-01	13668-110	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-110-01)
13668-110-05	13668-110	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-110-05)
13668-110-30	13668-110	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-110-30)
13668-109-01	13668-109	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-109-01)
13668-109-05	13668-109	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-109-05)
13668-109-30	13668-109	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-109-30)
13668-109-60	13668-109	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-109-60)
13668-111-01	13668-111	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-111-01)
13668-111-05	13668-111	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-111-05)
13668-111-30	13668-111	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20131211	N/A	ANDA	ANDA090774	Torrent Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (13668-111-30)
63187-457-30	63187-457	HUMAN PRESCRIPTION DRUG	Duloxetine hydrochloride	Duloxetin hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20190101	N/A	ANDA	ANDA090774	Proficient Rx LP	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-457-30)