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=ANDA207763"
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
68382-984-05 68382-984 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET, EXTENDED RELEASE ORAL 20200514 N/A ANDA ANDA207763 Zydus Pharmaceuticals USA Inc. LAMOTRIGINE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-984-05)
68382-984-06 68382-984 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET, EXTENDED RELEASE ORAL 20200514 N/A ANDA ANDA207763 Zydus Pharmaceuticals USA Inc. LAMOTRIGINE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-984-06)
68382-984-16 68382-984 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET, EXTENDED RELEASE ORAL 20200514 N/A ANDA ANDA207763 Zydus Pharmaceuticals USA Inc. LAMOTRIGINE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-984-16)
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