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=ANDA214124"
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
69918-380-30 69918-380 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220214 N/A ANDA ANDA214124 Amring Pharmaceuticals Inc. LAMOTRIGINE 200 mg/1 30 TABLET in 1 BOTTLE (69918-380-30)
69918-370-30 69918-370 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220214 N/A ANDA ANDA214124 Amring Pharmaceuticals Inc. LAMOTRIGINE 100 mg/1 30 TABLET in 1 BOTTLE (69918-370-30)
69918-360-30 69918-360 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220214 N/A ANDA ANDA214124 Amring Pharmaceuticals Inc. LAMOTRIGINE 50 mg/1 30 TABLET in 1 BOTTLE (69918-360-30)
69918-350-30 69918-350 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220214 N/A ANDA ANDA214124 Amring Pharmaceuticals Inc. LAMOTRIGINE 25 mg/1 30 TABLET in 1 BOTTLE (69918-350-30)
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