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=ANDA077653"
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
63629-3324-3 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20100203 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (63629-3324-3)
63629-3324-4 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20120202 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 28 TABLET in 1 BOTTLE (63629-3324-4)
63629-3324-5 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20140227 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 120 TABLET in 1 BOTTLE (63629-3324-5)
63629-3324-6 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20160304 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (63629-3324-6)
63629-3324-1 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230303 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 TABLET in 1 BOTTLE (63629-3324-1)
63629-3324-2 63629-3324 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20090216 N/A ANDA ANDA077653 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (63629-3324-2)
68001-156-00 68001-156 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20131125 N/A ANDA ANDA077653 BluePoint Laboratories VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (68001-156-00)
68001-160-00 68001-160 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20131125 N/A ANDA ANDA077653 BluePoint Laboratories VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (68001-160-00)
68071-2990-9 68071-2990 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230424 N/A ANDA ANDA077653 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (68071-2990-9)
68071-3431-0 68071-3431 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230727 N/A ANDA ANDA077653 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (68071-3431-0)
68001-157-00 68001-157 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20131125 N/A ANDA ANDA077653 BluePoint Laboratories VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (68001-157-00)
68084-844-01 68084-844 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20150513 N/A ANDA ANDA077653 American Health Packaging VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-844-01) / 1 TABLET in 1 BLISTER PACK (68084-844-11)
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)
68382-101-05 68382-101 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (68382-101-05)
68382-101-06 68382-101 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (68382-101-06)
68382-101-10 68382-101 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 1000 TABLET in 1 BOTTLE (68382-101-10)
68382-101-14 68382-101 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 60 TABLET in 1 BOTTLE (68382-101-14)
68382-101-16 68382-101 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20080613 N/A ANDA ANDA077653 Zydus Pharmaceuticals USA Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (68382-101-16)
68071-3432-0 68071-3432 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20230619 N/A ANDA ANDA077653 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (68071-3432-0)
63187-414-30 63187-414 HUMAN PRESCRIPTION DRUG Venlafaxine Venlafaxine TABLET ORAL 20190101 N/A ANDA ANDA077653 Proficient Rx LP VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (63187-414-30)
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