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
0904-6661-04 0904-6661 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Major Pharmaceuticals HALOPERIDOL 20 mg/1 30 BLISTER PACK in 1 CARTON (0904-6661-04) / 1 TABLET in 1 BLISTER PACK
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)
65841-628-01 65841-628 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 20 mg/1 100 TABLET in 1 BOTTLE (65841-628-01)
65841-628-06 65841-628 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 20 mg/1 30 TABLET in 1 BOTTLE (65841-628-06)
65841-837-01 65841-837 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL .5 mg/1 100 TABLET in 1 BOTTLE (65841-837-01)
65841-837-10 65841-837 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL .5 mg/1 1000 TABLET in 1 BOTTLE (65841-837-10)
65841-837-77 65841-837 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL .5 mg/1 10 BLISTER PACK in 1 CARTON (65841-837-77) / 10 TABLET in 1 BLISTER PACK (65841-837-30)
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)
67046-1255-3 67046-1255 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20241111 N/A ANDA ANDA077580 Coupler LLC HALOPERIDOL 1 mg/1 30 TABLET in 1 BLISTER PACK (67046-1255-3)
68382-079-01 68382-079 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL 5 mg/1 100 TABLET in 1 BOTTLE (68382-079-01)
68382-079-10 68382-079 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL 5 mg/1 1000 TABLET in 1 BOTTLE (68382-079-10)
68382-408-01 68382-408 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL 1 mg/1 100 TABLET in 1 BOTTLE (68382-408-01)
68382-408-10 68382-408 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL 1 mg/1 1000 TABLET in 1 BOTTLE (68382-408-10)
68382-408-77 68382-408 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Pharmaceuticals USA Inc. HALOPERIDOL 1 mg/1 10 BLISTER PACK in 1 CARTON (68382-408-77) / 10 TABLET in 1 BLISTER PACK (68382-408-30)
68084-249-01 68084-249 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080303 N/A ANDA ANDA077580 American Health Packaging HALOPERIDOL 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-249-01) / 1 TABLET in 1 BLISTER PACK (68084-249-11)
0904-6782-61 0904-6782 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20080103 N/A ANDA ANDA077580 Major Pharmaceuticals HALOPERIDOL 5 mg/1 100 BLISTER PACK in 1 CARTON (0904-6782-61) / 1 TABLET in 1 BLISTER PACK
65841-838-01 65841-838 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 1 mg/1 100 TABLET in 1 BOTTLE (65841-838-01)
65841-838-10 65841-838 HUMAN PRESCRIPTION DRUG Haloperidol Haloperidol TABLET ORAL 20230201 N/A ANDA ANDA077580 Zydus Lifesciences Limited HALOPERIDOL 1 mg/1 1000 TABLET in 1 BOTTLE (65841-838-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase