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
71610-637-30	71610-637	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220224	N/A	ANDA	ANDA076341	Aphena Pharma Solutions - Tennessee, LLC	PRAVASTATIN SODIUM	80 mg/1	30 TABLET in 1 BOTTLE (71610-637-30)
71610-637-45	71610-637	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220224	N/A	ANDA	ANDA076341	Aphena Pharma Solutions - Tennessee, LLC	PRAVASTATIN SODIUM	80 mg/1	45 TABLET in 1 BOTTLE (71610-637-45)
82009-007-10	82009-007	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20211203	N/A	ANDA	ANDA076341	Quallent	PRAVASTATIN SODIUM	40 mg/1	1000 TABLET in 1 BOTTLE (82009-007-10)
82009-007-90	82009-007	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20211203	N/A	ANDA	ANDA076341	Quallent	PRAVASTATIN SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (82009-007-90)
82009-008-05	82009-008	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20211203	N/A	ANDA	ANDA076341	Quallent	PRAVASTATIN SODIUM	80 mg/1	500 TABLET in 1 BOTTLE (82009-008-05)