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=ANDA208804"
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
69238-1344-1 69238-1344 HUMAN PRESCRIPTION DRUG Albuterol Albuterol TABLET ORAL 20180524 N/A ANDA ANDA208804 Amneal Pharmaceuticals NY LLC ALBUTEROL SULFATE 2 mg/1 100 TABLET in 1 BOTTLE (69238-1344-1)
69238-1344-5 69238-1344 HUMAN PRESCRIPTION DRUG Albuterol Albuterol TABLET ORAL 20180524 N/A ANDA ANDA208804 Amneal Pharmaceuticals NY LLC ALBUTEROL SULFATE 2 mg/1 500 TABLET in 1 BOTTLE (69238-1344-5)
69238-1345-1 69238-1345 HUMAN PRESCRIPTION DRUG Albuterol Albuterol TABLET ORAL 20180524 N/A ANDA ANDA208804 Amneal Pharmaceuticals NY LLC ALBUTEROL SULFATE 4 mg/1 100 TABLET in 1 BOTTLE (69238-1345-1)
69238-1345-5 69238-1345 HUMAN PRESCRIPTION DRUG Albuterol Albuterol TABLET ORAL 20180524 N/A ANDA ANDA208804 Amneal Pharmaceuticals NY LLC ALBUTEROL SULFATE 4 mg/1 500 TABLET in 1 BOTTLE (69238-1345-5)
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