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=ANDA210028"
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
70771-1373-1 70771-1373 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190312 N/A ANDA ANDA210028 Zydus Lifesciences Limited ATENOLOL; CHLORTHALIDONE 100 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70771-1373-1)
70771-1372-1 70771-1372 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190312 N/A ANDA ANDA210028 Zydus Lifesciences Limited ATENOLOL; CHLORTHALIDONE 50 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70771-1372-1)
16714-937-01 16714-937 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190326 N/A ANDA ANDA210028 Northstar Rx LLC. ATENOLOL; CHLORTHALIDONE 100 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (16714-937-01)
16714-936-01 16714-936 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190326 N/A ANDA ANDA210028 Northstar Rx LLC. ATENOLOL; CHLORTHALIDONE 50 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (16714-936-01)
70710-1167-1 70710-1167 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190312 N/A ANDA ANDA210028 Zydus Pharmaceuticals USA Inc. ATENOLOL; CHLORTHALIDONE 50 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70710-1167-1)
70710-1168-1 70710-1168 HUMAN PRESCRIPTION DRUG Atenolol and Chlorthalidone Atenolol and Chlorthalidone TABLET ORAL 20190312 N/A ANDA ANDA210028 Zydus Pharmaceuticals USA Inc. ATENOLOL; CHLORTHALIDONE 100 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (70710-1168-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase