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
70518-4065-0	70518-4065	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20240504	N/A	ANDA	ANDA216044	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4065-0)
64980-581-03	64980-581	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-581-03)
64980-581-09	64980-581	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-581-09)
64980-578-03	64980-578	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-578-03)
64980-578-09	64980-578	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-578-09)
64980-580-03	64980-580	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-580-03)
64980-580-09	64980-580	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-580-09)
70985-020-03	70985-020	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20231005	N/A	ANDA	ANDA216044	Drug Ocean LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-020-03)
70985-020-04	70985-020	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20231005	N/A	ANDA	ANDA216044	Drug Ocean LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-020-04)
64980-579-03	64980-579	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-579-03)
64980-579-09	64980-579	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221128	N/A	ANDA	ANDA216044	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-579-09)
70985-019-03	70985-019	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20231005	N/A	ANDA	ANDA216044	Drug Ocean LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-019-03)
70985-019-04	70985-019	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20231005	N/A	ANDA	ANDA216044	Drug Ocean LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70985-019-04)