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=BLA761122"
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
0173-0892-01 0173-0892 HUMAN PRESCRIPTION DRUG Nucala mepolizumab INJECTION, SOLUTION SUBCUTANEOUS 20190606 N/A BLA BLA761122 GlaxoSmithKline LLC MEPOLIZUMAB 100 mg/mL 1 SYRINGE in 1 CARTON (0173-0892-01) / 1 mL in 1 SYRINGE
0173-0892-42 0173-0892 HUMAN PRESCRIPTION DRUG Nucala mepolizumab INJECTION, SOLUTION SUBCUTANEOUS 20190606 N/A BLA BLA761122 GlaxoSmithKline LLC MEPOLIZUMAB 100 mg/mL 1 SYRINGE in 1 CARTON (0173-0892-42) / 1 mL in 1 SYRINGE
0173-0892-61 0173-0892 HUMAN PRESCRIPTION DRUG Nucala mepolizumab INJECTION, SOLUTION SUBCUTANEOUS 20190606 N/A BLA BLA761122 GlaxoSmithKline LLC MEPOLIZUMAB 100 mg/mL 1 SYRINGE in 1 CARTON (0173-0892-61) / 1 mL in 1 SYRINGE
0173-0892-63 0173-0892 HUMAN PRESCRIPTION DRUG Nucala mepolizumab INJECTION, SOLUTION SUBCUTANEOUS 20190606 N/A BLA BLA761122 GlaxoSmithKline LLC MEPOLIZUMAB 100 mg/mL 1 SYRINGE in 1 CARTON (0173-0892-63) / 1 mL in 1 SYRINGE
0173-0904-42 0173-0904 HUMAN PRESCRIPTION DRUG Nucala mepolizumab INJECTION, SOLUTION SUBCUTANEOUS 20220122 N/A BLA BLA761122 GlaxoSmithKline LLC MEPOLIZUMAB 40 mg/.4mL 1 SYRINGE in 1 CARTON (0173-0904-42) / .4 mL in 1 SYRINGE
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