| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63323-870-10 | 63323-870 | HUMAN PRESCRIPTION DRUG | Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE and SODIUM CHLORIDE | INJECTION, SOLUTION | INTRAVENOUS | 20201026 | N/A | ANDA | ANDA211211 | Fresenius Kabi USA, LLC | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE | 5 g/100mL; .9 g/100mL | 20 BAG in 1 CASE (63323-870-10) / 500 mL in 1 BAG (63323-870-01) |
| 63323-870-74 | 63323-870 | HUMAN PRESCRIPTION DRUG | Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE and SODIUM CHLORIDE | INJECTION, SOLUTION | INTRAVENOUS | 20201026 | N/A | ANDA | ANDA211211 | Fresenius Kabi USA, LLC | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE | 5 g/100mL; .9 g/100mL | 10 BAG in 1 CASE (63323-870-74) / 1000 mL in 1 BAG (63323-870-04) |