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=NDA020241"
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
0173-0594-02 0173-0594 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine KIT 20030929 N/A NDA NDA020241 GlaxoSmithKline LLC 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0594-02) / 1 KIT in 1 BLISTER PACK
0173-0642-55 0173-0642 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine TABLET ORAL 19950117 N/A NDA NDA020241 GlaxoSmithKline LLC LAMOTRIGINE 100 mg/1 100 TABLET in 1 BOTTLE (0173-0642-55)
0173-0644-60 0173-0644 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine TABLET ORAL 19950118 N/A NDA NDA020241 GlaxoSmithKline LLC LAMOTRIGINE 200 mg/1 60 TABLET in 1 BOTTLE (0173-0644-60)
0173-0633-10 0173-0633 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine TABLET ORAL 19960815 N/A NDA NDA020241 GlaxoSmithKline LLC LAMOTRIGINE 25 mg/1 35 TABLET in 1 DOSE PACK (0173-0633-10)
0173-0633-02 0173-0633 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine TABLET ORAL 19960815 N/A NDA NDA020241 GlaxoSmithKline LLC LAMOTRIGINE 25 mg/1 100 TABLET in 1 BOTTLE (0173-0633-02)
0173-0643-60 0173-0643 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine TABLET ORAL 19950117 N/A NDA NDA020241 GlaxoSmithKline LLC LAMOTRIGINE 150 mg/1 60 TABLET in 1 BOTTLE (0173-0643-60)
0173-0817-28 0173-0817 HUMAN PRESCRIPTION DRUG LAMICTAL lamotrigine KIT 20030929 N/A NDA NDA020241 GlaxoSmithKline LLC 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0817-28) / 1 KIT in 1 BLISTER PACK
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