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
46708-278-91	46708-278	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-91)
46708-279-10	46708-279	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	100 CAPSULE, DELAYED RELEASE in 1 CARTON (46708-279-10)
46708-279-30	46708-279	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-30)
46708-279-90	46708-279	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-90)
46708-279-91	46708-279	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-91)
46708-280-10	46708-280	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	100 CAPSULE, DELAYED RELEASE in 1 CARTON (46708-280-10)
46708-280-30	46708-280	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-30)
46708-280-90	46708-280	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-90)
46708-280-91	46708-280	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-91)
46708-278-60	46708-278	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-60)
46708-278-30	46708-278	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-30)
46708-278-10	46708-278	HUMAN PRESCRIPTION DRUG	DULOXETINE HYDROCHLORIDE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202949	Alembic Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 CARTON (46708-278-10)