美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=NDA019885"
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
0071-0535-23 0071-0535 HUMAN PRESCRIPTION DRUG Accupril quinapril hydrochloride TABLET, FILM COATED ORAL 19911119 N/A NDA NDA019885 Parke-Davis Div of Pfizer Inc QUINAPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0071-0535-23)
0071-0532-23 0071-0532 HUMAN PRESCRIPTION DRUG Accupril quinapril hydrochloride TABLET, FILM COATED ORAL 19911119 N/A NDA NDA019885 Parke-Davis Div of Pfizer Inc QUINAPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0071-0532-23)
0071-0530-23 0071-0530 HUMAN PRESCRIPTION DRUG Accupril quinapril hydrochloride TABLET, FILM COATED ORAL 19911119 N/A NDA NDA019885 Parke-Davis Div of Pfizer Inc QUINAPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0071-0530-23)
0071-0527-23 0071-0527 HUMAN PRESCRIPTION DRUG Accupril quinapril hydrochloride TABLET, FILM COATED ORAL 19911119 N/A NDA NDA019885 Parke-Davis Div of Pfizer Inc QUINAPRIL HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0071-0527-23)
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