| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1109-5 | 71335-1109 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20211220 | N/A | ANDA | ANDA203562 | Bryant Ranch Prepack | POTASSIUM CHLORIDE | 1500 mg/1 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-5) |
| 71335-1109-6 | 71335-1109 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20211220 | N/A | ANDA | ANDA203562 | Bryant Ranch Prepack | POTASSIUM CHLORIDE | 1500 mg/1 | 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-6) |
| 71335-1109-7 | 71335-1109 | HUMAN PRESCRIPTION DRUG | potassium chloride | potassium chloride | TABLET, EXTENDED RELEASE | ORAL | 20211220 | N/A | ANDA | ANDA203562 | Bryant Ranch Prepack | POTASSIUM CHLORIDE | 1500 mg/1 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-7) |
| 72189-462-30 | 72189-462 | HUMAN PRESCRIPTION DRUG | Potassium Chloride ER | Potassium Chloride ER | TABLET, EXTENDED RELEASE | ORAL | 20230417 | N/A | ANDA | ANDA203562 | Direct_Rx | POTASSIUM CHLORIDE | 1500 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-462-30) |