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
0093-7270-10	0093-7270	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20080929	20240930	ANDA	ANDA077793	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	80 mg/1	1000 TABLET in 1 BOTTLE (0093-7270-10)
0093-7270-98	0093-7270	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20080929	20240930	ANDA	ANDA077793	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (0093-7270-98)
43353-966-45	43353-966	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20140930	N/A	ANDA	ANDA077793	Aphena Pharma Solutions - Tennessee, LLC	PRAVASTATIN SODIUM	80 mg/1	45 TABLET in 1 BOTTLE (43353-966-45)
43353-966-60	43353-966	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20210120	N/A	ANDA	ANDA077793	Aphena Pharma Solutions - Tennessee, LLC	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (43353-966-60)
42291-669-10	42291-669	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20140630	N/A	ANDA	ANDA077793	AvKARE	PRAVASTATIN SODIUM	80 mg/1	1000 TABLET in 1 BOTTLE (42291-669-10)
42291-669-90	42291-669	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20140630	N/A	ANDA	ANDA077793	AvKARE	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (42291-669-90)
0480-7270-10	0480-7270	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230320	N/A	ANDA	ANDA077793	Teva Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	80 mg/1	1000 TABLET in 1 BOTTLE (0480-7270-10)
0480-7270-98	0480-7270	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230209	N/A	ANDA	ANDA077793	Teva Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (0480-7270-98)