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
72162-1711-5	72162-1711	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240404	N/A	ANDA	ANDA076341	Bryant Ranch Prepack	PRAVASTATIN SODIUM	80 mg/1	500 TABLET in 1 BOTTLE (72162-1711-5)
72162-1711-9	72162-1711	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240404	N/A	ANDA	ANDA076341	Bryant Ranch Prepack	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (72162-1711-9)
72162-2114-0	72162-2114	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20110718	N/A	ANDA	ANDA076341	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	1000 TABLET in 1 BOTTLE (72162-2114-0)
72789-143-30	72789-143	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20201022	N/A	ANDA	ANDA076341	PD-Rx Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-143-30)
72789-161-30	72789-161	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20210126	N/A	ANDA	ANDA076341	PD-Rx Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	40 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-161-30)
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)