| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 49884-849-01 | 49884-849 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20181029 | N/A | ANDA | ANDA207169 | Endo USA, Inc. | MIDODRINE HYDROCHLORIDE | 5 mg/1 | 100 TABLET in 1 BOTTLE (49884-849-01) |
| 63629-2227-1 | 63629-2227 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20210322 | N/A | ANDA | ANDA207169 | Bryant Ranch Prepack | MIDODRINE HYDROCHLORIDE | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (63629-2227-1) |
| 49884-874-01 | 49884-874 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20181029 | N/A | ANDA | ANDA207169 | Endo USA, Inc. | MIDODRINE HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (49884-874-01) |
| 72162-1517-1 | 72162-1517 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20231006 | N/A | ANDA | ANDA207169 | Bryant Ranch Prepack | MIDODRINE HYDROCHLORIDE | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (72162-1517-1) |
| 49884-814-01 | 49884-814 | HUMAN PRESCRIPTION DRUG | Midodrine Hydrochloride | Midodrine Hydrochloride | TABLET | ORAL | 20181029 | N/A | ANDA | ANDA207169 | Endo USA, Inc. | MIDODRINE HYDROCHLORIDE | 2.5 mg/1 | 100 TABLET in 1 BOTTLE (49884-814-01) |