| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-2411-1 | 71335-2411 | HUMAN PRESCRIPTION DRUG | RAMELTEON | RAMELTEON | TABLET, FILM COATED | ORAL | 20240610 | N/A | ANDA | ANDA215972 | Bryant Ranch Prepack | RAMELTEON | 8 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2411-1) |
| 71335-2411-2 | 71335-2411 | HUMAN PRESCRIPTION DRUG | RAMELTEON | RAMELTEON | TABLET, FILM COATED | ORAL | 20240610 | N/A | ANDA | ANDA215972 | Bryant Ranch Prepack | RAMELTEON | 8 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2411-2) |
| 59651-505-01 | 59651-505 | HUMAN PRESCRIPTION DRUG | RAMELTEON | RAMELTEON | TABLET, FILM COATED | ORAL | 20230710 | N/A | ANDA | ANDA215972 | Aurobindo Pharma Limited | RAMELTEON | 8 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-505-01) |
| 59651-505-30 | 59651-505 | HUMAN PRESCRIPTION DRUG | RAMELTEON | RAMELTEON | TABLET, FILM COATED | ORAL | 20230710 | N/A | ANDA | ANDA215972 | Aurobindo Pharma Limited | RAMELTEON | 8 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-505-30) |