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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
70771-1084-8 | 70771-1084 | HUMAN PRESCRIPTION DRUG | Mycophenolate Mofetil | Mycophenolate Mofetil | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | INTRAVENOUS | 20170922 | N/A | ANDA | ANDA204473 | Zydus Lifesciences Limited | MYCOPHENOLATE MOFETIL | 500 mg/20mL | 4 VIAL in 1 CARTON (70771-1084-8) / 20 mL in 1 VIAL |
68382-669-08 | 68382-669 | HUMAN PRESCRIPTION DRUG | Mycophenolate Mofetil | Mycophenolate Mofetil | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | INTRAVENOUS | 20170922 | N/A | ANDA | ANDA204473 | Zydus Pharmaceuticals USA Inc. | MYCOPHENOLATE MOFETIL | 500 mg/20mL | 4 VIAL in 1 CARTON (68382-669-08) / 20 mL in 1 VIAL |