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
63629-2100-1	63629-2100	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20191031	N/A	ANDA	ANDA209193	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BOTTLE (63629-2100-1)
72162-1089-3	72162-1089	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20231009	N/A	ANDA	ANDA209193	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BOTTLE (72162-1089-3)
63629-9284-1	63629-9284	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20220606	N/A	ANDA	ANDA209193	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET in 1 BOTTLE (63629-9284-1)
0527-2604-32	0527-2604	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20191226	N/A	ANDA	ANDA209193	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BOTTLE (0527-2604-32)
0527-2604-46	0527-2604	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20191226	N/A	ANDA	ANDA209193	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET in 1 BOTTLE (0527-2604-46)
0527-2605-32	0527-2605	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20191226	N/A	ANDA	ANDA209193	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET in 1 BOTTLE (0527-2605-32)
0527-2605-46	0527-2605	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20191226	N/A	ANDA	ANDA209193	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET in 1 BOTTLE (0527-2605-46)
42799-962-01	42799-962	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride, extended release	venlafaxine hydrochloride, extended release	TABLET	ORAL	20230315	N/A	ANDA	ANDA209193	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BOTTLE (42799-962-01)
42799-962-02	42799-962	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride, extended release	venlafaxine hydrochloride, extended release	TABLET	ORAL	20230315	N/A	ANDA	ANDA209193	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET in 1 BOTTLE (42799-962-02)
42799-963-01	42799-963	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride, extended release	venlafaxine hydrochloride, extended release	TABLET	ORAL	20230315	N/A	ANDA	ANDA209193	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET in 1 BOTTLE (42799-963-01)
42799-963-02	42799-963	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride, extended release	venlafaxine hydrochloride, extended release	TABLET	ORAL	20230315	N/A	ANDA	ANDA209193	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET in 1 BOTTLE (42799-963-02)
62135-531-30	62135-531	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	TABLET	ORAL	20230329	N/A	ANDA	ANDA209193	Chartwell RX, LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET in 1 BOTTLE (62135-531-30)