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=NDA022285"
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
50474-598-66 50474-598 HUMAN PRESCRIPTION DRUG Keppra XR levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20080924 N/A NDA NDA022285 UCB, Inc. LEVETIRACETAM 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-598-66)
50474-599-66 50474-599 HUMAN PRESCRIPTION DRUG Keppra XR levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20090401 N/A NDA NDA022285 UCB, Inc. LEVETIRACETAM 750 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-599-66)
70518-2109-0 70518-2109 HUMAN PRESCRIPTION DRUG Keppra XR levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190523 N/A NDA NDA022285 REMEDYREPACK INC. LEVETIRACETAM 500 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2109-0)
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