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
71335-9692-4	71335-9692	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20230418	N/A	ANDA	ANDA209869	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	60 TABLET in 1 BOTTLE (71335-9692-4)
71335-9692-5	71335-9692	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20230418	N/A	ANDA	ANDA209869	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	10 TABLET in 1 BOTTLE (71335-9692-5)
72162-1951-0	72162-1951	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20231025	N/A	ANDA	ANDA209869	Bryant Ranch Prepack	PRAVASTATIN SODIUM	10 mg/1	1000 TABLET in 1 BOTTLE (72162-1951-0)
50090-7892-0	50090-7892	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20260209	N/A	ANDA	ANDA209869	A-S Medication Solutions	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE (50090-7892-0)
82868-081-30	82868-081	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20250619	N/A	ANDA	ANDA209869	Northwind Health Company, LLC	PRAVASTATIN SODIUM	40 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-081-30)
50090-7892-1	50090-7892	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20260209	N/A	ANDA	ANDA209869	A-S Medication Solutions	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (50090-7892-1)
63629-8909-1	63629-8909	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20211119	N/A	ANDA	ANDA209869	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	1000 TABLET in 1 BOTTLE (63629-8909-1)
63629-8913-1	63629-8913	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20211119	N/A	ANDA	ANDA209869	Bryant Ranch Prepack	PRAVASTATIN SODIUM	80 mg/1	500 TABLET in 1 BOTTLE (63629-8913-1)