| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-2065-2 | 71335-2065 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20231019 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 5 mg/1 | 30 TABLET in 1 BOTTLE (71335-2065-2) |
| 71335-2065-3 | 71335-2065 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20240403 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 5 mg/1 | 60 TABLET in 1 BOTTLE (71335-2065-3) |
| 72162-2137-0 | 72162-2137 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20210629 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 10 mg/1 | 1000 TABLET in 1 BOTTLE (72162-2137-0) |
| 72162-2137-3 | 72162-2137 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20210629 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 10 mg/1 | 30 TABLET in 1 BOTTLE (72162-2137-3) |
| 72162-2137-5 | 72162-2137 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20210629 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 10 mg/1 | 500 TABLET in 1 BOTTLE (72162-2137-5) |
| 72162-2137-9 | 72162-2137 | HUMAN PRESCRIPTION DRUG | Donepezil Hydrochloride | Donepezil Hydrochloride | TABLET | ORAL | 20210629 | N/A | ANDA | ANDA078662 | Bryant Ranch Prepack | DONEPEZIL HYDROCHLORIDE | 10 mg/1 | 90 TABLET in 1 BOTTLE (72162-2137-9) |