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=ANDA078993"
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
60687-657-01 60687-657 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20220804 N/A ANDA ANDA078993 American Health Packaging LEVETIRACETAM 500 mg/1 100 BLISTER PACK in 1 CARTON (60687-657-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-657-11)
60687-668-01 60687-668 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20220804 N/A ANDA ANDA078993 American Health Packaging LEVETIRACETAM 1000 mg/1 100 BLISTER PACK in 1 CARTON (60687-668-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-668-11)
65862-315-05 65862-315 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20090115 N/A ANDA ANDA078993 Aurobindo Pharma Limited LEVETIRACETAM 1000 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-315-05)
65862-315-30 65862-315 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20090115 N/A ANDA ANDA078993 Aurobindo Pharma Limited LEVETIRACETAM 1000 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-315-30)
65862-315-60 65862-315 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20090115 N/A ANDA ANDA078993 Aurobindo Pharma Limited LEVETIRACETAM 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-315-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase