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=BLA103705"
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
50242-051-10 50242-051 HUMAN PRESCRIPTION DRUG Rituxan rituximab INJECTION, SOLUTION INTRAVENOUS 20190603 N/A BLA BLA103705 Genentech, Inc. RITUXIMAB 10 mg/mL 10 VIAL, SINGLE-USE in 1 CARTON (50242-051-10) / 10 mL in 1 VIAL, SINGLE-USE
50242-051-21 50242-051 HUMAN PRESCRIPTION DRUG Rituxan rituximab INJECTION, SOLUTION INTRAVENOUS 19971126 N/A BLA BLA103705 Genentech, Inc. RITUXIMAB 10 mg/mL 1 VIAL, SINGLE-USE in 1 CARTON (50242-051-21) / 10 mL in 1 VIAL, SINGLE-USE
50242-053-06 50242-053 HUMAN PRESCRIPTION DRUG Rituxan rituximab INJECTION, SOLUTION INTRAVENOUS 19971126 N/A BLA BLA103705 Genentech, Inc. RITUXIMAB 10 mg/mL 1 VIAL, SINGLE-USE in 1 CARTON (50242-053-06) / 50 mL in 1 VIAL, SINGLE-USE
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