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=ANDA203702"
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
60505-6151-4 60505-6151 HUMAN PRESCRIPTION DRUG Ceftriaxone Sodium Ceftriaxone Sodium INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20170630 N/A ANDA ANDA203702 Apotex Corp. CEFTRIAXONE SODIUM 250 mg/1 1 VIAL, SINGLE-USE in 1 CARTON (60505-6151-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
67184-1007-1 67184-1007 HUMAN PRESCRIPTION DRUG Ceftriaxone Sodium Ceftriaxone Sodium INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20160629 N/A ANDA ANDA203702 Qilu Pharmaceutical Co., Ltd. CEFTRIAXONE SODIUM 1 g/1 10 VIAL, SINGLE-USE in 1 CARTON (67184-1007-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
71205-545-01 71205-545 HUMAN PRESCRIPTION DRUG Ceftriaxone Sodium Ceftriaxone Sodium INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20210311 N/A ANDA ANDA203702 Proficient Rx LP CEFTRIAXONE SODIUM 1 g/1 1 VIAL, SINGLE-USE in 1 CARTON (71205-545-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
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