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=NDA022115"
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
0173-0757-00 0173-0757 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0757-00)
0173-0758-00 0173-0758 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine KIT 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0758-00) / 1 KIT in 1 BLISTER PACK
0173-0759-00 0173-0759 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine KIT 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0759-00) / 1 KIT in 1 BLISTER PACK
0173-0760-00 0173-0760 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine KIT 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0760-00) / 1 KIT in 1 BLISTER PACK
0173-0761-00 0173-0761 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110331 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0761-00)
0173-0756-00 0173-0756 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 100 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0756-00)
0173-0755-00 0173-0755 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 50 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0755-00)
0173-0754-00 0173-0754 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20090706 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0754-00)
0173-0781-00 0173-0781 HUMAN PRESCRIPTION DRUG LAMICTAL XR lamotrigine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110815 N/A NDA NDA022115 GlaxoSmithKline LLC LAMOTRIGINE 250 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0781-00)
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