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
71209-089-11	71209-089	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	225 mg/1	1000 TABLET, COATED in 1 BOTTLE (71209-089-11)
72241-075-04	72241-075	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, COATED in 1 BOTTLE (72241-075-04)
72241-075-11	72241-075	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 TABLET, COATED in 1 BOTTLE (72241-075-11)
72241-075-22	72241-075	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, COATED in 1 BOTTLE (72241-075-22)
75834-217-00	75834-217	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-00)
75834-217-30	75834-217	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-30)
75834-217-90	75834-217	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-90)