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
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)
71335-2507-3 71335-2507 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20241007 N/A ANDA ANDA078043 Bryant Ranch Prepack AMLODIPINE BESYLATE 10 mg/1 60 TABLET in 1 BOTTLE (71335-2507-3)
71335-2507-8 71335-2507 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20241007 N/A ANDA ANDA078043 Bryant Ranch Prepack AMLODIPINE BESYLATE 10 mg/1 180 TABLET in 1 BOTTLE (71335-2507-8)
71335-2507-9 71335-2507 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20241007 N/A ANDA ANDA078043 Bryant Ranch Prepack AMLODIPINE BESYLATE 10 mg/1 10 TABLET in 1 BOTTLE (71335-2507-9)
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