| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72819-234-99 | 72819-234 | HUMAN PRESCRIPTION DRUG | CUPRIC CHLORIDE | CUPRIC CHLORIDE | INJECTION, SOLUTION | INTRAVENOUS | 20241001 | N/A | ANDA | ANDA217626 | Archis Pharma LLC | CUPRIC CHLORIDE | .4 mg/mL | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96) |
| 72819-234-16 | 72819-234 | HUMAN PRESCRIPTION DRUG | CUPRIC CHLORIDE | CUPRIC CHLORIDE | INJECTION, SOLUTION | INTRAVENOUS | 20240705 | N/A | ANDA | ANDA217626 | Archis Pharma LLC | CUPRIC CHLORIDE | .4 mg/mL | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-06) |
| 72603-351-25 | 72603-351 | HUMAN PRESCRIPTION DRUG | CUPRIC CHLORIDE | CUPRIC CHLORIDE | INJECTION, SOLUTION | INTRAVENOUS | 20241001 | N/A | ANDA | ANDA217626 | Northstar Rx LLC | CUPRIC CHLORIDE | .4 mg/mL | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01) |