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
63187-414-60	63187-414	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20190101	N/A	ANDA	ANDA077653	Proficient Rx LP	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (63187-414-60)
63187-414-30	63187-414	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20190101	N/A	ANDA	ANDA077653	Proficient Rx LP	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (63187-414-30)
68001-159-00	68001-159	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (68001-159-00)
68001-160-00	68001-160	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (68001-160-00)
68001-157-00	68001-157	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (68001-157-00)
68001-156-00	68001-156	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (68001-156-00)
68001-158-00	68001-158	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68001-158-00)
68084-856-01	68084-856	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20150306	N/A	ANDA	ANDA077653	American Health Packaging	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)
68084-896-25	68084-896	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20150929	N/A	ANDA	ANDA077653	American Health Packaging	VENLAFAXINE HYDROCHLORIDE	25 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-896-25) / 1 TABLET in 1 BLISTER PACK (68084-896-95)
68084-844-01	68084-844	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20150513	N/A	ANDA	ANDA077653	American Health Packaging	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-844-01) / 1 TABLET in 1 BLISTER PACK (68084-844-11)
63629-3324-2	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20090216	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (63629-3324-2)
63629-3324-5	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20140227	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	120 TABLET in 1 BOTTLE (63629-3324-5)
63629-3324-6	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20160304	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (63629-3324-6)
63629-3324-3	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20100203	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (63629-3324-3)
63629-3324-1	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20230303	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (63629-3324-1)
63629-3324-4	63629-3324	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20120202	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	28 TABLET in 1 BOTTLE (63629-3324-4)
65841-671-01	65841-671	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (65841-671-01)
65841-671-14	65841-671	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (65841-671-14)
65841-671-16	65841-671	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (65841-671-16)
65841-672-01	65841-672	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (65841-672-01)