| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 30698-450-01 | 30698-450 | HUMAN PRESCRIPTION DRUG | Lotensin | benazepril hydrochloride | TABLET | ORAL | 19910621 | N/A | NDA | NDA019851 | Validus Pharmaceuticals LLC | BENAZEPRIL HYDROCHLORIDE | 40 mg/1 | 100 TABLET in 1 BOTTLE (30698-450-01) |
| 30698-449-01 | 30698-449 | HUMAN PRESCRIPTION DRUG | Lotensin | benazepril hydrochloride | TABLET | ORAL | 19910621 | N/A | NDA | NDA019851 | Validus Pharmaceuticals LLC | BENAZEPRIL HYDROCHLORIDE | 20 mg/1 | 100 TABLET in 1 BOTTLE (30698-449-01) |
| 30698-448-01 | 30698-448 | HUMAN PRESCRIPTION DRUG | Lotensin | benazepril hydrochloride | TABLET | ORAL | 19910621 | N/A | NDA | NDA019851 | Validus Pharmaceuticals LLC | BENAZEPRIL HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (30698-448-01) |