| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 62135-487-90 | 62135-487 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril | TABLET, FILM COATED | ORAL | 20231106 | N/A | ANDA | ANDA076803 | Chartwell RX, LLC | QUINAPRIL HYDROCHLORIDE | 40 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-487-90) |
| 62135-486-90 | 62135-486 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril | TABLET, FILM COATED | ORAL | 20231106 | N/A | ANDA | ANDA076803 | Chartwell RX, LLC | QUINAPRIL HYDROCHLORIDE | 20 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-486-90) |
| 62135-485-90 | 62135-485 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril | TABLET, FILM COATED | ORAL | 20231106 | N/A | ANDA | ANDA076803 | Chartwell RX, LLC | QUINAPRIL HYDROCHLORIDE | 10 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-485-90) |
| 62135-484-60 | 62135-484 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril | TABLET, FILM COATED | ORAL | 20231106 | N/A | ANDA | ANDA076803 | Chartwell RX, LLC | QUINAPRIL HYDROCHLORIDE | 5 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (62135-484-60) |