| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82293-005-10 | 82293-005 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231018 | N/A | ANDA | ANDA211973 | Novugen Pharma (USA) LLC | MIDODRINE HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (82293-005-10) |
| 82293-003-10 | 82293-003 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231018 | N/A | ANDA | ANDA211973 | Novugen Pharma (USA) LLC | MIDODRINE HYDROCHLORIDE | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (82293-003-10) |
| 82293-004-10 | 82293-004 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231018 | N/A | ANDA | ANDA211973 | Novugen Pharma (USA) LLC | MIDODRINE HYDROCHLORIDE | 5 mg/1 | 100 TABLET in 1 BOTTLE (82293-004-10) |
| 67046-1404-3 | 67046-1404 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20241108 | N/A | ANDA | ANDA211973 | Coupler LLC | MIDODRINE HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BLISTER PACK (67046-1404-3) |