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=ANDA065372"
符合检索条件的记录共 2 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
63323-321-12 63323-321 HUMAN PRESCRIPTION DRUG POLYMYXIN B POLYMYXIN B SULFATE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC 20091117 N/A ANDA ANDA065372 Fresenius Kabi USA, LLC POLYMYXIN B SULFATE 500000 [USP'U]/1 10 VIAL in 1 TRAY (63323-321-12) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-02)
63323-321-10 63323-321 HUMAN PRESCRIPTION DRUG POLYMYXIN B POLYMYXIN B SULFATE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC 20091117 N/A ANDA ANDA065372 Fresenius Kabi USA, LLC POLYMYXIN B SULFATE 500000 [USP'U]/1 10 VIAL in 1 TRAY (63323-321-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase