| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70069-822-01 | 70069-822 | HUMAN PRESCRIPTION DRUG | Prucalopride succinate | Prucalopride succinate | TABLET | ORAL | 20250624 | N/A | ANDA | ANDA219078 | Somerset Therapeutics, LLC | PRUCALOPRIDE SUCCINATE | 2 mg/1 | 1 BOTTLE in 1 BOTTLE (70069-822-01) / 30 TABLET in 1 BOTTLE |
| 70069-821-01 | 70069-821 | HUMAN PRESCRIPTION DRUG | Prucalopride succinate | Prucalopride succinate | TABLET | ORAL | 20250624 | N/A | ANDA | ANDA219078 | Somerset Therapeutics, LLC | PRUCALOPRIDE SUCCINATE | 1 mg/1 | 1 BOTTLE in 1 BOTTLE (70069-821-01) / 30 TABLET in 1 BOTTLE |