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=BLA761043"
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
49401-088-02 49401-088 HUMAN PRESCRIPTION DRUG BENLYSTA belimumab SOLUTION SUBCUTANEOUS 20170720 N/A BLA BLA761043 GlaxoSmithKline LLC BELIMUMAB 200 mg/mL 1 SYRINGE in 1 CARTON (49401-088-02) / 1 mL in 1 SYRINGE (49401-088-01)
49401-088-35 49401-088 HUMAN PRESCRIPTION DRUG BENLYSTA belimumab SOLUTION SUBCUTANEOUS 20170720 N/A BLA BLA761043 GlaxoSmithKline LLC BELIMUMAB 200 mg/mL 4 SYRINGE in 1 CARTON (49401-088-35) / 1 mL in 1 SYRINGE (49401-088-01)
49401-088-47 49401-088 HUMAN PRESCRIPTION DRUG BENLYSTA belimumab SOLUTION SUBCUTANEOUS 20170720 N/A BLA BLA761043 GlaxoSmithKline LLC BELIMUMAB 200 mg/mL 4 SYRINGE in 1 CARTON (49401-088-47) / 1 mL in 1 SYRINGE (49401-088-42)
49401-088-50 49401-088 HUMAN PRESCRIPTION DRUG BENLYSTA belimumab SOLUTION SUBCUTANEOUS 20170720 N/A BLA BLA761043 GlaxoSmithKline LLC BELIMUMAB 200 mg/mL 1 SYRINGE in 1 CARTON (49401-088-50) / 1 mL in 1 SYRINGE (49401-088-42)
49401-088-61 49401-088 HUMAN PRESCRIPTION DRUG BENLYSTA belimumab SOLUTION SUBCUTANEOUS 20200602 N/A BLA BLA761043 GlaxoSmithKline LLC BELIMUMAB 200 mg/mL 1 SYRINGE in 1 CARTON (49401-088-61) / 1 mL in 1 SYRINGE
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