| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-2724-0 | 70518-2724 | HUMAN PRESCRIPTION DRUG | Buspirone Hydrochloride | Buspirone Hydrochloride | TABLET | ORAL | 20200505 | N/A | ANDA | ANDA204582 | REMEDYREPACK INC. | BUSPIRONE HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BLISTER PACK (70518-2724-0) |
| 70518-1940-0 | 70518-1940 | HUMAN PRESCRIPTION DRUG | Buspirone Hydrochloride | Buspirone Hydrochloride | TABLET | ORAL | 20190307 | N/A | ANDA | ANDA204582 | REMEDYREPACK INC. | BUSPIRONE HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BLISTER PACK (70518-1940-0) |
| 67046-0558-3 | 67046-0558 | HUMAN PRESCRIPTION DRUG | Buspirone Hydrochloride | Buspirone Hydrochloride | TABLET | ORAL | 20241108 | N/A | ANDA | ANDA204582 | Coupler LLC | BUSPIRONE HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BLISTER PACK (67046-0558-3) |