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=ANDA077580"
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
48433-151-20 48433-151 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20260601 N/A ANDA ANDA077580 Safecor Health, LLC HALOPERIDOL .5 mg/1 100 BLISTER PACK in 1 CARTON (48433-151-20) / 1 TABLET in 1 BLISTER PACK (48433-151-01)
65841-626-01 65841-626 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 5 mg/1 100 TABLET in 1 BOTTLE (65841-626-01)
65841-626-10 65841-626 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 5 mg/1 1000 TABLET in 1 BOTTLE (65841-626-10)
68382-407-01 68382-407 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL .5 mg/1 100 TABLET in 1 BOTTLE (68382-407-01)
68382-407-10 68382-407 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL .5 mg/1 1000 TABLET in 1 BOTTLE (68382-407-10)
68382-407-77 68382-407 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL .5 mg/1 10 BLISTER PACK in 1 CARTON (68382-407-77) / 10 TABLET in 1 BLISTER PACK (68382-407-30)
60687-161-01 60687-161 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20160309 N/A ANDA ANDA077580 American Health Packaging HALOPERIDOL 5 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-161-01) / 1 TABLET in 1 BLISTER PACK (60687-161-11)
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