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=ANDA091237"
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
25000-136-71 25000-136 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20151106 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1000 TABLET in 1 BOTTLE (25000-136-71)
25000-136-93 25000-136 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20151106 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BAG in 1 BOX (25000-136-93) / 37470 TABLET in 1 BAG
25000-136-98 25000-136 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20151106 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BAG in 1 BOX (25000-136-98) / 34065 TABLET in 1 BAG
25000-135-30 25000-135 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20151106 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 6 BAG in 1 BOX (25000-135-30) / 6500 TABLET in 1 BAG
25000-135-02 25000-135 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20191220 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (25000-135-02) / 24 TABLET in 1 BOTTLE
25000-135-03 25000-135 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20151106 N/A ANDA ANDA091237 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 30 TABLET in 1 BOTTLE (25000-135-03)
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