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 |