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
55154-5370-0	55154-5370	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20120210	20260831	ANDA	ANDA076056	Cardinal Health 107, LLC	PRAVASTATIN SODIUM	40 mg/1	10 BLISTER PACK in 1 BAG (55154-5370-0) / 1 TABLET in 1 BLISTER PACK
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)
68071-3788-9	68071-3788	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20250203	N/A	ANDA	ANDA076056	NuCare Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (68071-3788-9)
70518-4408-0	70518-4408	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20250728	N/A	ANDA	ANDA076056	REMEDYREPACK INC.	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BLISTER PACK (70518-4408-0)
70518-4408-1	70518-4408	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20250824	N/A	ANDA	ANDA076056	REMEDYREPACK INC.	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4408-1)