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=ANDA205897"
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
43817-240-01 43817-240 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20171016 N/A ANDA ANDA205897 Panacea Biotec Limited PRASUGREL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43817-240-01)
43817-239-01 43817-239 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20171016 N/A ANDA ANDA205897 Panacea Biotec Limited PRASUGREL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43817-239-01)
60505-4643-3 60505-4643 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20171016 N/A ANDA ANDA205897 Apotex Corp. PRASUGREL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-4643-3)
60505-4642-3 60505-4642 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20171016 N/A ANDA ANDA205897 Apotex Corp. PRASUGREL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-4642-3)
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