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=ANDA078043"
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
68180-720-09 68180-720 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20180815 20251231 ANDA ANDA078043 Lupin Pharmaceuticals, Inc. AMLODIPINE BESYLATE 5 mg/1 90 TABLET in 1 BOTTLE (68180-720-09)
50090-5355-0 50090-5355 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20201111 N/A ANDA ANDA078043 A-S Medication Solutions AMLODIPINE BESYLATE 10 mg/1 90 TABLET in 1 BOTTLE (50090-5355-0)
68180-719-09 68180-719 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20181031 20260131 ANDA ANDA078043 Lupin Pharmaceuticals, Inc. AMLODIPINE BESYLATE 2.5 mg/1 90 TABLET in 1 BOTTLE (68180-719-09)
68071-3698-9 68071-3698 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20241011 N/A ANDA ANDA078043 NuCare Pharmaceuticals,Inc. AMLODIPINE BESYLATE 10 mg/1 90 TABLET in 1 BOTTLE (68071-3698-9)
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