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
33342-160-09	33342-160	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-09)
33342-160-10	33342-160	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-10)
33342-160-12	33342-160	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (33342-160-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
33342-160-44	33342-160	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-160-44)
33342-161-07	33342-161	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-07)
33342-161-10	33342-161	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-10)
33342-161-12	33342-161	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	10 BLISTER PACK in 1 CARTON (33342-161-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
33342-161-44	33342-161	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-44)
33342-162-07	33342-162	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-07)
33342-162-10	33342-162	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-10)
33342-162-12	33342-162	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	10 BLISTER PACK in 1 CARTON (33342-162-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
33342-162-44	33342-162	HUMAN PRESCRIPTION DRUG	Duloxetine Hydrochloride	Duloxetine Hydrochloride	CAPSULE, DELAYED RELEASE	ORAL	20170324	N/A	ANDA	ANDA204815	Macleods Pharmaceuticals Limited	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-44)