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=ANDA078858"
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
13668-014-05 13668-014 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078858 Torrent Pharmaceuticals Limited LEVETIRACETAM 250 mg/1 500 TABLET in 1 BOTTLE (13668-014-05)
13668-014-12 13668-014 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078858 Torrent Pharmaceuticals Limited LEVETIRACETAM 250 mg/1 120 TABLET in 1 BOTTLE (13668-014-12)
13668-014-25 13668-014 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078858 Torrent Pharmaceuticals Limited LEVETIRACETAM 250 mg/1 250 TABLET in 1 BOTTLE (13668-014-25)
13668-014-31 13668-014 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078858 Torrent Pharmaceuticals Limited LEVETIRACETAM 250 mg/1 2500 TABLET in 1 BOTTLE (13668-014-31)
13668-014-60 13668-014 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078858 Torrent Pharmaceuticals Limited LEVETIRACETAM 250 mg/1 60 TABLET in 1 BOTTLE (13668-014-60)
69102-105-01 69102-105 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20201028 N/A ANDA ANDA078858 OWP Pharmaceuticals, Inc. LEVETIRACETAM 500 mg/1 120 TABLET in 1 BOTTLE (69102-105-01)
69102-106-01 69102-106 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20201028 N/A ANDA ANDA078858 OWP Pharmaceuticals, Inc. LEVETIRACETAM 750 mg/1 120 TABLET in 1 BOTTLE (69102-106-01)
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