| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70756-049-11 | 70756-049 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231101 | N/A | ANDA | ANDA217271 | Lifestar Pharma LLC | MIDODRINE HYDROCHLORIDE | 5 mg/1 | 100 TABLET in 1 BOTTLE (70756-049-11) |
| 70756-050-11 | 70756-050 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231101 | N/A | ANDA | ANDA217271 | Lifestar Pharma LLC | MIDODRINE HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (70756-050-11) |
| 70756-010-11 | 70756-010 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231101 | N/A | ANDA | ANDA217271 | Lifestar Pharma LLC | MIDODRINE HYDROCHLORIDE | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (70756-010-11) |