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=ANDA078904"
符合检索条件的记录共 5 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
55111-248-01 55111-248 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078904 Dr. Reddy's Laboratories Limited LEVETIRACETAM 1000 mg/1 100 TABLET in 1 BOTTLE (55111-248-01)
55111-248-05 55111-248 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078904 Dr. Reddy's Laboratories Limited LEVETIRACETAM 1000 mg/1 500 TABLET in 1 BOTTLE (55111-248-05)
55111-248-30 55111-248 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078904 Dr. Reddy's Laboratories Limited LEVETIRACETAM 1000 mg/1 30 TABLET in 1 BOTTLE (55111-248-30)
55111-248-60 55111-248 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078904 Dr. Reddy's Laboratories Limited LEVETIRACETAM 1000 mg/1 60 TABLET in 1 BOTTLE (55111-248-60)
55111-248-79 55111-248 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET ORAL 20090115 N/A ANDA ANDA078904 Dr. Reddy's Laboratories Limited LEVETIRACETAM 1000 mg/1 1 BLISTER PACK in 1 CARTON (55111-248-79) / 10 TABLET in 1 BLISTER PACK
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