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=ANDA091261"
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
60429-349-60 60429-349 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-Release levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121031 N/A ANDA ANDA091261 Golden State Medical Supply, Inc. LEVETIRACETAM 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-349-60)
60429-350-60 60429-350 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-Release levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130305 N/A ANDA ANDA091261 Golden State Medical Supply, Inc. LEVETIRACETAM 750 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-350-60)
60505-3280-5 60505-3280 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091261 Apotex Corp. LEVETIRACETAM 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-5)
60505-3280-6 60505-3280 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091261 Apotex Corp. LEVETIRACETAM 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-6)
60505-3280-8 60505-3280 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091261 Apotex Corp. LEVETIRACETAM 500 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-8)
60505-3517-5 60505-3517 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091261 Apotex Corp. LEVETIRACETAM 750 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3517-5)
60505-3517-6 60505-3517 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110912 N/A ANDA ANDA091261 Apotex Corp. LEVETIRACETAM 750 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3517-6)
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