| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 68382-246-01 | 68382-246 | HUMAN PRESCRIPTION DRUG | Ethacrynate Sodium | Ethacrynate Sodium | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | INTRAVENOUS | 20180124 | N/A | ANDA | ANDA207758 | Zydus Pharmaceuticals USA Inc. | ETHACRYNATE SODIUM | 50 mg/50mL | 1 VIAL in 1 CARTON (68382-246-01) / 50 mL in 1 VIAL |
| 70771-1106-1 | 70771-1106 | HUMAN PRESCRIPTION DRUG | Ethacrynate Sodium | Ethacrynate Sodium | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | INTRAVENOUS | 20180124 | N/A | ANDA | ANDA207758 | Zydus Lifesciences Limited | ETHACRYNATE SODIUM | 50 mg/50mL | 1 VIAL in 1 CARTON (70771-1106-1) / 50 mL in 1 VIAL |