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
50090-3898-1	50090-3898	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20170216	N/A	ANDA	ANDA207068	A-S Medication Solutions	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (50090-3898-1)
71335-0296-1	71335-0296	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220705	N/A	ANDA	ANDA207068	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE (71335-0296-1)
71335-0296-2	71335-0296	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220705	N/A	ANDA	ANDA207068	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (71335-0296-2)
71335-0296-3	71335-0296	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220705	N/A	ANDA	ANDA207068	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	100 TABLET in 1 BOTTLE (71335-0296-3)
71335-0296-4	71335-0296	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220705	N/A	ANDA	ANDA207068	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	60 TABLET in 1 BOTTLE (71335-0296-4)
71335-0296-5	71335-0296	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20220705	N/A	ANDA	ANDA207068	Bryant Ranch Prepack	PRAVASTATIN SODIUM	20 mg/1	10 TABLET in 1 BOTTLE (71335-0296-5)
71205-121-30	71205-121	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20180904	N/A	ANDA	ANDA207068	Proficient Rx LP	PRAVASTATIN SODIUM	40 mg/1	30 TABLET in 1 BOTTLE (71205-121-30)
71205-121-60	71205-121	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20180904	N/A	ANDA	ANDA207068	Proficient Rx LP	PRAVASTATIN SODIUM	40 mg/1	60 TABLET in 1 BOTTLE (71205-121-60)
71205-121-90	71205-121	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20180904	N/A	ANDA	ANDA207068	Proficient Rx LP	PRAVASTATIN SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (71205-121-90)