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"
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
60760-304-30 60760-304 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200616 N/A ANDA ANDA090555 St. Mary's Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)
71335-1104-1 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20190220 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 TABLET in 1 BOTTLE (71335-1104-1)
71335-1104-2 71335-1104 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20190213 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (71335-1104-2)
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)
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)
65862-407-01 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (65862-407-01)
65862-407-10 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (65862-407-10) / 10 TABLET in 1 BLISTER PACK
65862-407-30 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (65862-407-30)
65862-407-71 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 7000 TABLET in 1 BOTTLE (65862-407-71)
65862-407-90 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (65862-407-90)
65862-407-99 65862-407 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine Hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Aurobindo Pharma Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 TABLET in 1 BOTTLE (65862-407-99)
67046-0557-3 67046-0557 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20241107 N/A ANDA ANDA090555 Coupler LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BLISTER PACK (67046-0557-3)
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)
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)
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