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=ANDA202821"
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
65862-621-99 65862-621 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20171103 N/A ANDA ANDA202821 Aurobindo Pharma Limited FLECAINIDE ACETATE 50 mg/1 1000 TABLET in 1 BOTTLE (65862-621-99)
57237-063-01 57237-063 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20150708 N/A ANDA ANDA202821 Rising Pharma Holdings, Inc. FLECAINIDE ACETATE 50 mg/1 100 TABLET in 1 BOTTLE (57237-063-01)
65862-623-01 65862-623 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20171103 N/A ANDA ANDA202821 Aurobindo Pharma Limited FLECAINIDE ACETATE 150 mg/1 100 TABLET in 1 BOTTLE (65862-623-01)
65862-623-30 65862-623 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20171103 N/A ANDA ANDA202821 Aurobindo Pharma Limited FLECAINIDE ACETATE 150 mg/1 30 TABLET in 1 BOTTLE (65862-623-30)
65862-623-99 65862-623 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20171103 N/A ANDA ANDA202821 Aurobindo Pharma Limited FLECAINIDE ACETATE 150 mg/1 1000 TABLET in 1 BOTTLE (65862-623-99)
50090-5306-0 50090-5306 HUMAN PRESCRIPTION DRUG Flecainide Acetate Flecainide Acetate TABLET ORAL 20201028 N/A ANDA ANDA202821 A-S Medication Solutions FLECAINIDE ACETATE 50 mg/1 60 TABLET in 1 BOTTLE (50090-5306-0)
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