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=ANDA217337"
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
62135-714-60 62135-714 HUMAN PRESCRIPTION DRUG Mesalamine Mesalamine TABLET, DELAYED RELEASE ORAL 20230721 N/A ANDA ANDA217337 Chartwell RX, LLC MESALAMINE 1.2 g/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-714-60)
62135-714-12 62135-714 HUMAN PRESCRIPTION DRUG Mesalamine Mesalamine TABLET, DELAYED RELEASE ORAL 20230721 N/A ANDA ANDA217337 Chartwell RX, LLC MESALAMINE 1.2 g/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-714-12)
72162-2213-2 72162-2213 HUMAN PRESCRIPTION DRUG MESALAMINE mesalamine TABLET, DELAYED RELEASE ORAL 20240529 N/A ANDA ANDA217337 Bryant Ranch Prepack MESALAMINE 1.2 g/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2213-2)
0527-3012-48 0527-3012 HUMAN PRESCRIPTION DRUG MESALAMINE mesalamine TABLET, DELAYED RELEASE ORAL 20230603 N/A ANDA ANDA217337 Lannett Company Inc. MESALAMINE 1.2 g/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (0527-3012-48)
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