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=ANDA077987"
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
69097-788-12 69097-788 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 10 mg/1 500 TABLET in 1 BOTTLE (69097-788-12)
69097-789-05 69097-789 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE (69097-789-05)
69097-789-12 69097-789 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 20 mg/1 500 TABLET in 1 BOTTLE (69097-789-12)
69097-791-05 69097-791 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 40 mg/1 90 TABLET in 1 BOTTLE (69097-791-05)
69097-791-12 69097-791 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 40 mg/1 500 TABLET in 1 BOTTLE (69097-791-12)
69097-792-05 69097-792 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 80 mg/1 90 TABLET in 1 BOTTLE (69097-792-05)
69097-792-12 69097-792 HUMAN PRESCRIPTION DRUG PRAVASTATIN SODIUM PRAVASTATIN SODIUM TABLET ORAL 20240601 N/A ANDA ANDA077987 CIPLA USA INC. PRAVASTATIN SODIUM 80 mg/1 500 TABLET in 1 BOTTLE (69097-792-12)
50090-5809-0 50090-5809 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20211015 N/A ANDA ANDA077987 A-S Medication Solutions PRAVASTATIN SODIUM 80 mg/1 30 TABLET in 1 BOTTLE (50090-5809-0)
50090-5809-1 50090-5809 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20211015 N/A ANDA ANDA077987 A-S Medication Solutions PRAVASTATIN SODIUM 80 mg/1 90 TABLET in 1 BOTTLE (50090-5809-1)
55700-994-30 55700-994 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20230111 N/A ANDA ANDA077987 Quality Care Products, LLC PRAVASTATIN SODIUM 40 mg/1 30 TABLET in 1 BOTTLE (55700-994-30)
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