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=ANDA210683"
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
76385-147-01 76385-147 HUMAN PRESCRIPTION DRUG Flecainide Acetate flecainide acetate TABLET ORAL 20240115 N/A ANDA ANDA210683 Bayshore Pharmaceuticals LLC FLECAINIDE ACETATE 150 mg/1 100 TABLET in 1 BOTTLE (76385-147-01)
72789-385-01 72789-385 HUMAN PRESCRIPTION DRUG Flecainide Acetate flecainide acetate TABLET ORAL 20240227 N/A ANDA ANDA210683 PD-Rx Pharmaceuticals, Inc. FLECAINIDE ACETATE 50 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-385-01)
72789-385-60 72789-385 HUMAN PRESCRIPTION DRUG Flecainide Acetate flecainide acetate TABLET ORAL 20240227 N/A ANDA ANDA210683 PD-Rx Pharmaceuticals, Inc. FLECAINIDE ACETATE 50 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (72789-385-60)
72789-385-93 72789-385 HUMAN PRESCRIPTION DRUG Flecainide Acetate flecainide acetate TABLET ORAL 20240227 N/A ANDA ANDA210683 PD-Rx Pharmaceuticals, Inc. FLECAINIDE ACETATE 50 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (72789-385-93)
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