| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82804-034-30 | 82804-034 | HUMAN PRESCRIPTION DRUG | lurasidone hydrochloride | lurasidone hydrochloride | TABLET, FILM COATED | ORAL | 20231101 | N/A | ANDA | ANDA212091 | Proficient Rx LP | LURASIDONE HYDROCHLORIDE | 20 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-034-30) |
| 82804-034-60 | 82804-034 | HUMAN PRESCRIPTION DRUG | lurasidone hydrochloride | lurasidone hydrochloride | TABLET, FILM COATED | ORAL | 20231101 | N/A | ANDA | ANDA212091 | Proficient Rx LP | LURASIDONE HYDROCHLORIDE | 20 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (82804-034-60) |
| 82804-034-90 | 82804-034 | HUMAN PRESCRIPTION DRUG | lurasidone hydrochloride | lurasidone hydrochloride | TABLET, FILM COATED | ORAL | 20231101 | N/A | ANDA | ANDA212091 | Proficient Rx LP | LURASIDONE HYDROCHLORIDE | 20 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-034-90) |
| 50090-7078-0 | 50090-7078 | HUMAN PRESCRIPTION DRUG | lurasidone hydrochloride | lurasidone hydrochloride | TABLET, FILM COATED | ORAL | 20240131 | N/A | ANDA | ANDA212091 | A-S Medication Solutions | LURASIDONE HYDROCHLORIDE | 20 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7078-0) |