| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-0854-2 | 71335-0854 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20220309 | N/A | ANDA | ANDA076820 | Bryant Ranch Prepack | BENAZEPRIL HYDROCHLORIDE | 10 mg/1 | 60 TABLET in 1 BOTTLE (71335-0854-2) |
| 71335-0854-3 | 71335-0854 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20220411 | N/A | ANDA | ANDA076820 | Bryant Ranch Prepack | BENAZEPRIL HYDROCHLORIDE | 10 mg/1 | 100 TABLET in 1 BOTTLE (71335-0854-3) |
| 71335-0854-4 | 71335-0854 | HUMAN PRESCRIPTION DRUG | Benazepril Hydrochloride | Benazepril Hydrochloride | TABLET | ORAL | 20180611 | N/A | ANDA | ANDA076820 | Bryant Ranch Prepack | BENAZEPRIL HYDROCHLORIDE | 10 mg/1 | 90 TABLET in 1 BOTTLE (71335-0854-4) |