| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63187-914-60 | 63187-914 | HUMAN PRESCRIPTION DRUG | AMLODIPINE BESYLATE | AMLODIPINE BESYLATE | TABLET | ORAL | 20171002 | N/A | ANDA | ANDA077073 | Proficient Rx LP | AMLODIPINE BESYLATE | 10 mg/1 | 60 TABLET in 1 BOTTLE (63187-914-60) |
| 63187-914-90 | 63187-914 | HUMAN PRESCRIPTION DRUG | AMLODIPINE BESYLATE | AMLODIPINE BESYLATE | TABLET | ORAL | 20171002 | N/A | ANDA | ANDA077073 | Proficient Rx LP | AMLODIPINE BESYLATE | 10 mg/1 | 90 TABLET in 1 BOTTLE (63187-914-90) |
| 70518-0835-3 | 70518-0835 | HUMAN PRESCRIPTION DRUG | AMLODIPINE BESYLATE | AMLODIPINE BESYLATE | TABLET | ORAL | 20230608 | N/A | ANDA | ANDA077073 | REMEDYREPACK INC. | AMLODIPINE BESYLATE | 5 mg/1 | 30 TABLET in 1 BLISTER PACK (70518-0835-3) |
| 51655-044-52 | 51655-044 | HUMAN PRESCRIPTION DRUG | AMLODIPINE BESYLATE | AMLODIPINE BESYLATE | TABLET | ORAL | 20231130 | N/A | ANDA | ANDA077073 | Northwind Health Company, LLC | AMLODIPINE BESYLATE | 5 mg/1 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-044-52) |