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=ANDA076056"
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
71205-294-60 71205-294 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20190701 N/A ANDA ANDA076056 Proficient Rx LP PRAVASTATIN SODIUM 40 mg/1 60 TABLET in 1 BOTTLE (71205-294-60)
71205-294-90 71205-294 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20190701 N/A ANDA ANDA076056 Proficient Rx LP PRAVASTATIN SODIUM 40 mg/1 90 TABLET in 1 BOTTLE (71205-294-90)
50090-6898-0 50090-6898 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20231211 N/A ANDA ANDA076056 A-S Medication Solutions PRAVASTATIN SODIUM 20 mg/1 90 TABLET in 1 BOTTLE (50090-6898-0)
51079-458-20 51079-458 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20060522 20260831 ANDA ANDA076056 Mylan Institutional Inc. PRAVASTATIN SODIUM 20 mg/1 100 BLISTER PACK in 1 CARTON (51079-458-20) / 1 TABLET in 1 BLISTER PACK (51079-458-01)
51079-782-20 51079-782 HUMAN PRESCRIPTION DRUG Pravastatin Sodium Pravastatin Sodium TABLET ORAL 20071003 20260831 ANDA ANDA076056 Mylan Institutional Inc. PRAVASTATIN SODIUM 40 mg/1 100 BLISTER PACK in 1 CARTON (51079-782-20) / 1 TABLET in 1 BLISTER PACK (51079-782-01)
82868-096-30 82868-096 HUMAN PRESCRIPTION DRUG Pravastatin sodium Pravastatin sodium TABLET ORAL 20251219 N/A ANDA ANDA076056 Northwind Health Company, LLC PRAVASTATIN SODIUM 40 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (82868-096-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase