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
68382-018-06	68382-018	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (68382-018-06)
68382-018-10	68382-018	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (68382-018-10)
68382-018-14	68382-018	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (68382-018-14)
68382-018-16	68382-018	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (68382-018-16)
67046-1124-3	67046-1124	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20241111	N/A	ANDA	ANDA077653	Coupler LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BLISTER PACK (67046-1124-3)
60760-121-30	60760-121	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20110130	N/A	ANDA	ANDA077653	St. Marys Medical Park Pharmacy	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)
65841-673-01	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (65841-673-01)
68382-019-01	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68382-019-01)
68382-019-05	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	500 TABLET in 1 BOTTLE (68382-019-05)
68382-019-06	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (68382-019-06)
68382-019-10	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 TABLET in 1 BOTTLE (68382-019-10)
68382-019-14	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (68382-019-14)
68382-019-16	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (68382-019-16)
67046-1397-3	67046-1397	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20241112	N/A	ANDA	ANDA077653	Coupler LLC	VENLAFAXINE HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BLISTER PACK (67046-1397-3)
60760-728-60	60760-728	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20230421	N/A	ANDA	ANDA077653	ST. MARY'S MEDICAL PARK PHARMACY	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60)
68382-101-01	68382-101	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (68382-101-01)
68382-020-10	68382-020	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (68382-020-10)
68382-020-14	68382-020	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	50 mg/1	60 TABLET in 1 BOTTLE (68382-020-14)
68382-020-16	68382-020	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (68382-020-16)
68084-896-25	68084-896	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20150929	N/A	ANDA	ANDA077653	American Health Packaging	VENLAFAXINE HYDROCHLORIDE	25 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-896-25) / 1 TABLET in 1 BLISTER PACK (68084-896-95)