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
71335-1104-3	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200103	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (71335-1104-3)
71335-1104-4	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20211228	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	28 TABLET in 1 BOTTLE (71335-1104-4)
71335-1104-5	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20211228	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	120 TABLET in 1 BOTTLE (71335-1104-5)
71335-1104-6	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20211228	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (71335-1104-6)
71335-1213-1	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (71335-1213-1)
71335-1213-2	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (71335-1213-2)
71335-1213-3	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (71335-1213-3)
71335-1213-4	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	10 TABLET in 1 BOTTLE (71335-1213-4)