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=NDA011719"
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
61703-124-40 61703-124 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate INJECTION, SOLUTION INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS 20221017 N/A NDA NDA011719 Hospira, Inc. METHOTREXATE SODIUM 25 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-124-40) / 40 mL in 1 VIAL, SINGLE-DOSE
61703-350-38 61703-350 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20050727 N/A NDA NDA011719 Hospira, Inc. METHOTREXATE SODIUM 25 mg/mL 5 VIAL, MULTI-DOSE in 1 CARTON (61703-350-38) / 2 mL in 1 VIAL, MULTI-DOSE (61703-350-37)
61703-350-10 61703-350 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20140925 N/A NDA NDA011719 Hospira, Inc. METHOTREXATE SODIUM 25 mg/mL 5 VIAL, MULTI-DOSE in 1 CARTON (61703-350-10) / 2 mL in 1 VIAL, MULTI-DOSE (61703-350-09)
61703-408-41 61703-408 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate INJECTION, SOLUTION INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS 20010226 N/A NDA NDA011719 Hospira, Inc. METHOTREXATE SODIUM 25 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-41) / 40 mL in 1 VIAL, SINGLE-DOSE
61703-408-25 61703-408 HUMAN PRESCRIPTION DRUG Methotrexate Methotrexate INJECTION, SOLUTION INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS 20131111 N/A NDA NDA011719 Hospira, Inc. METHOTREXATE SODIUM 25 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-25) / 40 mL in 1 VIAL, SINGLE-DOSE
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