产品NDC |
产品类型 |
商品名 |
通用名 |
剂型 |
给药途径 |
上市日期 |
市场分类 |
申请号 |
标签持有者 |
活性成分 |
规格 |
规格单位 |
71335-0232 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | Bryant Ranch Prepack | PHENYTOIN SODIUM | 100 | mg/1 |
63187-891 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | Proficient Rx LP | PHENYTOIN SODIUM | 100 | mg/1 |
70518-0981 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20180122 | ANDA | ANDA040621 | REMEDYREPACK INC. | PHENYTOIN SODIUM | 100 | mg/1 |
62756-402 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | Sun Pharmaceutical Industries, Inc. | PHENYTOIN SODIUM | 100 | mg/1 |
53002-1501 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | RPK Pharmaceuticals, Inc. | PHENYTOIN SODIUM | 100 | mg/1 |
63629-6364 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | Bryant Ranch Prepack | PHENYTOIN SODIUM | 100 | mg/1 |
63629-6382 | HUMAN PRESCRIPTION DRUG | PHENYTOIN SODIUM | PHENYTOIN SODIUM | CAPSULE, EXTENDED RELEASE | ORAL | 20061212 | ANDA | ANDA040621 | Bryant Ranch Prepack | PHENYTOIN SODIUM | 100 | mg/1 |