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
84386-031-99	84386-031	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20250227	N/A	ANDA	ANDA076056	Aurobindo Pharma Limited	PRAVASTATIN SODIUM	10 mg/1	1000 TABLET in 1 BOTTLE (84386-031-99)
50090-7947-0	50090-7947	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20260401	N/A	ANDA	ANDA076056	A-S Medication Solutions	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE (50090-7947-0)
50090-7947-1	50090-7947	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20260401	N/A	ANDA	ANDA076056	A-S Medication Solutions	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (50090-7947-1)
50090-4206-0	50090-4206	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20190321	N/A	ANDA	ANDA076056	A-S Medication Solutions	PRAVASTATIN SODIUM	40 mg/1	30 TABLET in 1 BOTTLE (50090-4206-0)
68071-3895-9	68071-3895	HUMAN PRESCRIPTION DRUG	Pravastatin sodium	Pravastatin sodium	TABLET	ORAL	20250916	N/A	ANDA	ANDA076056	NuCare Pharmaceuticals, Inc.	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (68071-3895-9)
50090-4206-1	50090-4206	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20190321	N/A	ANDA	ANDA076056	A-S Medication Solutions	PRAVASTATIN SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (50090-4206-1)
51655-343-52	51655-343	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230228	20260930	ANDA	ANDA076056	Northwind Health Company, LLC	PRAVASTATIN SODIUM	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-343-52)