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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
71335-2389-7 | 71335-2389 | HUMAN PRESCRIPTION DRUG | PREDNISONE | PREDNISONE | TABLET | ORAL | 20240529 | N/A | ANDA | ANDA215672 | Bryant Ranch Prepack | PREDNISONE | 50 mg/1 | 20 TABLET in 1 BOTTLE (71335-2389-7) |
71335-2389-8 | 71335-2389 | HUMAN PRESCRIPTION DRUG | PREDNISONE | PREDNISONE | TABLET | ORAL | 20240529 | N/A | ANDA | ANDA215672 | Bryant Ranch Prepack | PREDNISONE | 50 mg/1 | 10 TABLET in 1 BOTTLE (71335-2389-8) |
59651-486-78 | 59651-486 | HUMAN PRESCRIPTION DRUG | PREDNISONE | PREDNISONE | TABLET | ORAL | 20220328 | N/A | ANDA | ANDA215672 | Aurobindo Pharma Limited | PREDNISONE | 5 mg/1 | 10 BLISTER PACK in 1 CARTON (59651-486-78) / 10 TABLET in 1 BLISTER PACK |
71335-2356-1 | 71335-2356 | HUMAN PRESCRIPTION DRUG | PREDNISONE | PREDNISONE | TABLET | ORAL | 20240528 | N/A | ANDA | ANDA215672 | Bryant Ranch Prepack | PREDNISONE | 2.5 mg/1 | 30 TABLET in 1 BOTTLE (71335-2356-1) |
71335-2356-2 | 71335-2356 | HUMAN PRESCRIPTION DRUG | PREDNISONE | PREDNISONE | TABLET | ORAL | 20240528 | N/A | ANDA | ANDA215672 | Bryant Ranch Prepack | PREDNISONE | 2.5 mg/1 | 90 TABLET in 1 BOTTLE (71335-2356-2) |