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=ANDA215560"
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
70954-391-10 70954-391 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20211025 N/A ANDA ANDA215560 ANI Pharmaceuticals, Inc. ATENOLOL; CHLORTHALIDONE 100 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70954-391-10)
70954-390-10 70954-390 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20211025 N/A ANDA ANDA215560 ANI Pharmaceuticals, Inc. ATENOLOL; CHLORTHALIDONE 50 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70954-390-10)
10135-733-01 10135-733 HUMAN PRESCRIPTION DRUG ATENOLOL AND CHLORTHALIDONE atenolol and chlorthalidone tablet TABLET ORAL 20220301 N/A ANDA ANDA215560 MARLEX PHARMACEUTICALS, INC ATENOLOL; CHLORTHALIDONE 50 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (10135-733-01)
10135-734-01 10135-734 HUMAN PRESCRIPTION DRUG ATENOLOL AND CHLORTHALIDONE atenolol and chlorthalidone tablet TABLET ORAL 20220301 N/A ANDA ANDA215560 MARLEX PHARMACEUTICALS, INC ATENOLOL; CHLORTHALIDONE 100 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (10135-734-01)
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