| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1781-2 | 71335-1781 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20210625 | N/A | ANDA | ANDA203562 | Bryant Ranch Prepack | POTASSIUM CHLORIDE | 750 mg/1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-2) |
| 71335-1781-3 | 71335-1781 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20210309 | N/A | ANDA | ANDA203562 | Bryant Ranch Prepack | POTASSIUM CHLORIDE | 750 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-3) |
| 67296-2131-2 | 67296-2131 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20160726 | N/A | ANDA | ANDA203562 | Redpharm Drug | POTASSIUM CHLORIDE | 1500 mg/1 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2) |
| 50090-7456-0 | 50090-7456 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20241114 | N/A | ANDA | ANDA203562 | A-S Medication Solutions | POTASSIUM CHLORIDE | 1500 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7456-0) |