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
50771-001-02	50771-001	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20160906	N/A	ANDA	ANDA202036	Yaopharma Co., Ltd.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50771-001-02)
50771-002-02	50771-002	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20160906	N/A	ANDA	ANDA202036	Yaopharma Co., Ltd.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50771-002-02)
50771-003-02	50771-003	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20160906	N/A	ANDA	ANDA202036	Yaopharma Co., Ltd.	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50771-003-02)
50771-004-02	50771-004	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20160906	N/A	ANDA	ANDA202036	Yaopharma Co., Ltd.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50771-004-02)
50771-005-02	50771-005	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20160906	N/A	ANDA	ANDA202036	Yaopharma Co., Ltd.	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50771-005-02)
61919-406-60	61919-406	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	VENLAFAXINE	TABLET	ORAL	20171031	N/A	ANDA	ANDA202036	DIRECT RX	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (61919-406-60)