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=NDA021759"
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
0955-1727-20 0955-1727 HUMAN PRESCRIPTION DRUG OXALIPLATIN oxaliplatin INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20140707 20250131 NDA AUTHORIZED GENERIC NDA021759 Winthrop U.S, a business of sanofi-aventis U.S. LLC OXALIPLATIN 5 mg/mL 1 VIAL, GLASS in 1 CARTON (0955-1727-20) / 20 mL in 1 VIAL, GLASS
0955-1733-20 0955-1733 HUMAN PRESCRIPTION DRUG OXALIPLATIN oxaliplatin INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20150901 N/A NDA AUTHORIZED GENERIC NDA021759 Winthrop U.S, a business of sanofi-aventis U.S. LLC OXALIPLATIN 5 mg/mL 1 VIAL, GLASS in 1 CARTON (0955-1733-20) / 20 mL in 1 VIAL, GLASS
0955-1731-10 0955-1731 HUMAN PRESCRIPTION DRUG OXALIPLATIN oxaliplatin INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20150901 N/A NDA AUTHORIZED GENERIC NDA021759 Winthrop U.S, a business of sanofi-aventis U.S. LLC OXALIPLATIN 5 mg/mL 1 VIAL, GLASS in 1 CARTON (0955-1731-10) / 10 mL in 1 VIAL, GLASS
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