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=ANDA090540"
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
71335-0080-5 71335-0080 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel Bisulfate TABLET, FILM COATED ORAL 20240529 N/A ANDA ANDA090540 Bryant Ranch Prepack CLOPIDOGREL BISULFATE 75 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0080-5)
71205-073-30 71205-073 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel Bisulfate TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090540 Proficient Rx LP CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-073-30)
71205-073-60 71205-073 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel Bisulfate TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090540 Proficient Rx LP CLOPIDOGREL BISULFATE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-073-60)
71205-073-90 71205-073 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel Bisulfate TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090540 Proficient Rx LP CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-073-90)
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