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=ANDA215307"
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
51655-403-52 51655-403 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20230413 N/A ANDA ANDA215307 Northwind Pharmaceuticals, LLC DIGOXIN .125 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-403-52)
70954-200-10 70954-200 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220825 N/A ANDA ANDA215307 Novitium Pharma LLC DIGOXIN .0625 mg/1 100 TABLET in 1 BOTTLE (70954-200-10)
70954-201-10 70954-201 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20211122 N/A ANDA ANDA215307 Novitium Pharma LLC DIGOXIN .125 mg/1 100 TABLET in 1 BOTTLE (70954-201-10)
70954-201-20 70954-201 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20211122 N/A ANDA ANDA215307 Novitium Pharma LLC DIGOXIN .125 mg/1 1000 TABLET in 1 BOTTLE (70954-201-20)
70954-202-10 70954-202 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20211122 N/A ANDA ANDA215307 Novitium Pharma LLC DIGOXIN .25 mg/1 100 TABLET in 1 BOTTLE (70954-202-10)
70954-202-20 70954-202 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20211122 N/A ANDA ANDA215307 Novitium Pharma LLC DIGOXIN .25 mg/1 1000 TABLET in 1 BOTTLE (70954-202-20)
10135-747-01 10135-747 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220601 N/A ANDA ANDA215307 Marlex Pharmaceuticals, Inc. DIGOXIN .125 mg/1 100 TABLET in 1 BOTTLE (10135-747-01)
10135-747-10 10135-747 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220601 N/A ANDA ANDA215307 Marlex Pharmaceuticals, Inc. DIGOXIN .125 mg/1 1000 TABLET in 1 BOTTLE (10135-747-10)
10135-748-01 10135-748 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220601 N/A ANDA ANDA215307 Marlex Pharmaceuticals, Inc. DIGOXIN .25 mg/1 100 TABLET in 1 BOTTLE (10135-748-01)
10135-748-10 10135-748 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220601 N/A ANDA ANDA215307 Marlex Pharmaceuticals, Inc. DIGOXIN .25 mg/1 1000 TABLET in 1 BOTTLE (10135-748-10)
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