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=NDA204417"
符合检索条件的记录共 6 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
80705-101-02 80705-101 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1500 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210929 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1500 mg/1 1 BLISTER PACK in 1 CARTON (80705-101-02) / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
80705-101-30 80705-101 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1500 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210212 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80705-101-30)
80705-101-99 80705-101 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1500 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210212 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1500 mg/1 1 BLISTER PACK in 1 CARTON (80705-101-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
80705-100-02 80705-100 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1000 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210929 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1000 mg/1 1 BLISTER PACK in 1 CARTON (80705-100-02) / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
80705-100-30 80705-100 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1000 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210212 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1000 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80705-100-30)
80705-100-99 80705-100 HUMAN PRESCRIPTION DRUG ELEPSIA XR 1000 MG levetiracetam TABLET, EXTENDED RELEASE ORAL 20210212 N/A NDA NDA204417 TRIPOINT THERAPEUTICS, LLC LEVETIRACETAM 1000 mg/1 1 BLISTER PACK in 1 CARTON (80705-100-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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