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=ANDA213351"
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
52605-083-05 52605-083 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel TABLET ORAL 20210301 N/A ANDA ANDA213351 POLYGEN PHARMACEUTICALS INC. CLOPIDOGREL BISULFATE 300 mg/1 500 TABLET in 1 BOTTLE, DISPENSING (52605-083-05)
52605-083-13 52605-083 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel TABLET ORAL 20210301 N/A ANDA ANDA213351 POLYGEN PHARMACEUTICALS INC. CLOPIDOGREL BISULFATE 300 mg/1 30 TABLET in 1 BOTTLE (52605-083-13)
52605-082-13 52605-082 HUMAN PRESCRIPTION DRUG clopidogrel clopidogrel TABLET ORAL 20210301 N/A ANDA ANDA213351 POLYGEN PHARMACEUTICALS INC. CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET in 1 BOTTLE (52605-082-13)
52605-082-10 52605-082 HUMAN PRESCRIPTION DRUG clopidogrel clopidogrel TABLET ORAL 20210301 N/A ANDA ANDA213351 POLYGEN PHARMACEUTICALS INC. CLOPIDOGREL BISULFATE 75 mg/1 1000 TABLET in 1 BOTTLE, DISPENSING (52605-082-10)
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