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
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)
75834-218-00	75834-218	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-218-00)
75834-218-30	75834-218	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-218-30)
75834-218-90	75834-218	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-218-90)
75834-219-00	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-00)
75834-219-30	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-30)
75834-219-90	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-90)
71209-087-01	71209-087	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, COATED in 1 BOTTLE (71209-087-01)
71209-087-04	71209-087	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, COATED in 1 BOTTLE (71209-087-04)
71209-087-11	71209-087	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 TABLET, COATED in 1 BOTTLE (71209-087-11)
71209-088-01	71209-088	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, COATED in 1 BOTTLE (71209-088-01)
71209-088-04	71209-088	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, COATED in 1 BOTTLE (71209-088-04)
71209-088-11	71209-088	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	1000 TABLET, COATED in 1 BOTTLE (71209-088-11)
71209-089-01	71209-089	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, COATED in 1 BOTTLE (71209-089-01)
71209-089-04	71209-089	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, COATED in 1 BOTTLE (71209-089-04)
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)
70518-3136-0	70518-3136	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210630	N/A	ANDA	ANDA211323	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3136-0)