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
71209-087-11	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)