| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 65162-754-10 | 65162-754 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20100202 | N/A | ANDA | ANDA076820 | Amneal Pharmaceuticals LLC | BENAZEPRIL HYDROCHLORIDE | 40 mg/1 | 100 TABLET in 1 BOTTLE (65162-754-10) |
| 65162-754-50 | 65162-754 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20100202 | N/A | ANDA | ANDA076820 | Amneal Pharmaceuticals LLC | BENAZEPRIL HYDROCHLORIDE | 40 mg/1 | 500 TABLET in 1 BOTTLE (65162-754-50) |
| 71205-244-90 | 71205-244 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20190301 | N/A | ANDA | ANDA076820 | Proficient Rx LP | BENAZEPRIL HYDROCHLORIDE | 20 mg/1 | 90 TABLET in 1 BOTTLE (71205-244-90) |