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）
检索条件:" 注册申请号=ANDA090555"
符合检索条件的记录共 72 条，共 4 页，当前第 3 页 ，可点击列名称排序
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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
57237-173-01 57237-173 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (57237-173-01)
57237-173-90 57237-173 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (57237-173-90)
50090-4853-0 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (50090-4853-0)
50090-4853-1 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (50090-4853-1)
57237-174-01 57237-174 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (57237-174-01)
57237-174-90 57237-174 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (57237-174-90)
70518-1385-2 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20210201 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-1385-2)
70518-1385-3 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20231107 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3)
65862-408-01 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (65862-408-01)
70518-2652-0 70518-2652 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200325 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-2652-0)
70518-2652-1 70518-2652 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200327 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BLISTER PACK (70518-2652-1)
70518-2652-2 70518-2652 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20201223 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-2652-2)
57237-172-01 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (57237-172-01)
57237-172-90 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (57237-172-90)
57237-176-01 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (57237-176-01)
57237-176-90 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (57237-176-90)
65862-408-10 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (65862-408-10) / 10 TABLET in 1 BLISTER PACK
65862-408-20 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 20 TABLET in 1 BOTTLE (65862-408-20)
65862-408-66 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 6000 TABLET in 1 BOTTLE (65862-408-66)
65862-408-90 65862-408 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (65862-408-90)
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