| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 42799-954-01 | 42799-954 | HUMAN PRESCRIPTION DRUG | Donepezil hydrochloride | Donepezil hydrochloride | TABLET, FILM COATED | ORAL | 20231205 | N/A | ANDA | ANDA203713 | Edenbridge Pharmaceuticals LLC. | DONEPEZIL HYDROCHLORIDE | 23 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (42799-954-01) |
| 42799-954-02 | 42799-954 | HUMAN PRESCRIPTION DRUG | Donepezil hydrochloride | Donepezil hydrochloride | TABLET, FILM COATED | ORAL | 20231205 | N/A | ANDA | ANDA203713 | Edenbridge Pharmaceuticals LLC. | DONEPEZIL HYDROCHLORIDE | 23 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (42799-954-02) |