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=ANDA213412"
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
50090-5183-1 50090-5183 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20200928 N/A ANDA ANDA213412 A-S Medication Solutions CHLORTHALIDONE 50 mg/1 30 TABLET in 1 BOTTLE (50090-5183-1)
71335-2580-1 71335-2580 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20250206 N/A ANDA ANDA213412 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 90 TABLET in 1 BOTTLE (71335-2580-1)
71335-2580-2 71335-2580 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20250206 N/A ANDA ANDA213412 Bryant Ranch Prepack CHLORTHALIDONE 50 mg/1 30 TABLET in 1 BOTTLE (71335-2580-2)
50090-6126-2 50090-6126 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220930 N/A ANDA ANDA213412 A-S Medication Solutions CHLORTHALIDONE 25 mg/1 90 TABLET in 1 BOTTLE (50090-6126-2)
50090-6126-1 50090-6126 HUMAN PRESCRIPTION DRUG Chlorthalidone Chlorthalidone TABLET ORAL 20220930 N/A ANDA ANDA213412 A-S Medication Solutions CHLORTHALIDONE 25 mg/1 30 TABLET in 1 BOTTLE (50090-6126-1)
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