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=ANDA207252"
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
57884-3042-1 57884-3042 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20170809 N/A ANDA ANDA207252 Jiangsu Hengrui Pharmaceuticals Co., Ltd. DOCETAXEL 80 mg/4mL 1 VIAL, GLASS in 1 CARTON (57884-3042-1) / 4 mL in 1 VIAL, GLASS
25021-245-01 25021-245 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel Anhydrous INJECTION, SOLUTION INTRAVENOUS 20170915 N/A ANDA ANDA207252 Sagent Pharmaceuticals DOCETAXEL ANHYDROUS 20 mg/mL 1 VIAL in 1 CARTON (25021-245-01) / 1 mL in 1 VIAL
25021-245-04 25021-245 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel Anhydrous INJECTION, SOLUTION INTRAVENOUS 20170915 N/A ANDA ANDA207252 Sagent Pharmaceuticals DOCETAXEL ANHYDROUS 20 mg/mL 1 VIAL in 1 CARTON (25021-245-04) / 4 mL in 1 VIAL
57884-3043-1 57884-3043 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20170809 N/A ANDA ANDA207252 Jiangsu Hengrui Pharmaceuticals Co., Ltd. DOCETAXEL 160 mg/8mL 1 VIAL, GLASS in 1 CARTON (57884-3043-1) / 8 mL in 1 VIAL, GLASS
57884-3041-1 57884-3041 HUMAN PRESCRIPTION DRUG Docetaxel Docetaxel INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20170809 N/A ANDA ANDA207252 Jiangsu Hengrui Pharmaceuticals Co., Ltd. DOCETAXEL 20 mg/mL 1 VIAL, GLASS in 1 CARTON (57884-3041-1) / 1 mL in 1 VIAL, GLASS
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