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
0093-7201-10	0093-7201	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20060425	20261231	ANDA	ANDA076056	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	20 mg/1	1000 TABLET in 1 BOTTLE (0093-7201-10)
0093-7201-98	0093-7201	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20060425	20260831	ANDA	ANDA076056	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (0093-7201-98)
0093-7202-10	0093-7202	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20060425	20260930	ANDA	ANDA076056	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	40 mg/1	1000 TABLET in 1 BOTTLE (0093-7202-10)
43353-964-45	43353-964	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20140926	N/A	ANDA	ANDA076056	Aphena Pharma Solutions - Tennessee, LLC	PRAVASTATIN SODIUM	40 mg/1	45 TABLET in 1 BOTTLE (43353-964-45)
0093-7202-98	0093-7202	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20060425	20260930	ANDA	ANDA076056	Teva Pharmaceuticals USA, Inc.	PRAVASTATIN SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (0093-7202-98)
68788-8871-3	68788-8871	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20250430	N/A	ANDA	ANDA076056	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE (68788-8871-3)
68788-8871-6	68788-8871	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20250430	N/A	ANDA	ANDA076056	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	20 mg/1	60 TABLET in 1 BOTTLE (68788-8871-6)
68788-8871-9	68788-8871	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20250430	N/A	ANDA	ANDA076056	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (68788-8871-9)