| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 65862-620-99 | 65862-620 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril Hydrochloride | TABLET, FILM COATED | ORAL | 20130429 | N/A | ANDA | ANDA202725 | Aurobindo Pharma Limited | QUINAPRIL HYDROCHLORIDE | 40 mg/1 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-620-99) |
| 65862-617-55 | 65862-617 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril Hydrochloride | TABLET, FILM COATED | ORAL | 20130429 | N/A | ANDA | ANDA202725 | Aurobindo Pharma Limited | QUINAPRIL HYDROCHLORIDE | 5 mg/1 | 15000 TABLET, FILM COATED in 1 BOTTLE (65862-617-55) |
| 65862-617-30 | 65862-617 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril Hydrochloride | TABLET, FILM COATED | ORAL | 20130429 | N/A | ANDA | ANDA202725 | Aurobindo Pharma Limited | QUINAPRIL HYDROCHLORIDE | 5 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-617-30) |
| 65862-617-90 | 65862-617 | HUMAN PRESCRIPTION DRUG | Quinapril | Quinapril Hydrochloride | TABLET, FILM COATED | ORAL | 20130429 | N/A | ANDA | ANDA202725 | Aurobindo Pharma Limited | QUINAPRIL HYDROCHLORIDE | 5 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-617-90) |