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）

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)