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=BLA125472"
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
50242-138-01 50242-138 HUMAN PRESCRIPTION DRUG Actemra tocilizumab INJECTION, SOLUTION SUBCUTANEOUS 20131021 N/A BLA BLA125472 Genentech, Inc. TOCILIZUMAB 162 mg/.9mL 1 SYRINGE, GLASS in 1 BOX (50242-138-01) / .9 mL in 1 SYRINGE, GLASS
50242-138-86 50242-138 HUMAN PRESCRIPTION DRUG Actemra tocilizumab INJECTION, SOLUTION SUBCUTANEOUS 20131021 N/A BLA BLA125472 Genentech, Inc. TOCILIZUMAB 162 mg/.9mL 1 SYRINGE, GLASS in 1 BOX (50242-138-86) / .9 mL in 1 SYRINGE, GLASS
50242-143-01 50242-143 HUMAN PRESCRIPTION DRUG Actemra ACTPen tocilizumab INJECTION, SOLUTION SUBCUTANEOUS 20181119 N/A BLA BLA125472 Genentech, Inc. TOCILIZUMAB 162 mg/.9mL 1 SYRINGE, GLASS in 1 BOX (50242-143-01) / .9 mL in 1 SYRINGE, GLASS
50242-143-86 50242-143 HUMAN PRESCRIPTION DRUG Actemra ACTPen tocilizumab INJECTION, SOLUTION SUBCUTANEOUS 20181119 N/A BLA BLA125472 Genentech, Inc. TOCILIZUMAB 162 mg/.9mL 1 SYRINGE, GLASS in 1 BOX (50242-143-86) / .9 mL in 1 SYRINGE, GLASS
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