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
65841-673-05	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	500 TABLET in 1 BOTTLE (65841-673-05)
65841-673-06	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BOTTLE (65841-673-06)
65841-673-10	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (65841-673-10)
65841-673-14	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	60 TABLET in 1 BOTTLE (65841-673-14)
65841-673-16	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (65841-673-16)
60760-121-30	60760-121	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20110130	N/A	ANDA	ANDA077653	St. Marys Medical Park Pharmacy	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)
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)
68071-3432-0	68071-3432	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20230619	N/A	ANDA	ANDA077653	NuCare Pharmaceuticals,Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (68071-3432-0)
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)
68382-019-01	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68382-019-01)
68382-019-05	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	500 TABLET in 1 BOTTLE (68382-019-05)
68382-019-06	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (68382-019-06)
68382-019-10	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 TABLET in 1 BOTTLE (68382-019-10)
68382-019-14	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (68382-019-14)
68382-019-16	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (68382-019-16)
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)
65841-672-05	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	500 TABLET in 1 BOTTLE (65841-672-05)
65841-672-06	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	30 TABLET in 1 BOTTLE (65841-672-06)
65841-672-10	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	1000 TABLET in 1 BOTTLE (65841-672-10)