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=ANDA091399"
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
68001-114-06 68001-114 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, EXTENDED RELEASE ORAL 20140213 N/A ANDA ANDA091399 BluePoint Laboratories LEVETIRACETAM 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-114-06)
68001-113-06 68001-113 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, EXTENDED RELEASE ORAL 20140213 N/A ANDA ANDA091399 BluePoint Laboratories LEVETIRACETAM 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-113-06)
68180-117-07 68180-117 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091399 Lupin Pharmaceuticals, Inc. LEVETIRACETAM 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-117-07)
68180-118-07 68180-118 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091399 Lupin Pharmaceuticals, Inc. LEVETIRACETAM 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-118-07)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase