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
0615-8539-39	0615-8539	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20241119	20261031	ANDA	ANDA077987	NCS HealthCare of KY, LLC dba Vangard Labs	PRAVASTATIN SODIUM	10 mg/1	30 TABLET in 1 BLISTER PACK (0615-8539-39)
55700-994-30	55700-994	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230111	20261031	ANDA	ANDA077987	Quality Care Products, LLC	PRAVASTATIN SODIUM	40 mg/1	30 TABLET in 1 BOTTLE (55700-994-30)
68788-8425-3	68788-8425	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230417	N/A	ANDA	ANDA077987	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	10 mg/1	30 TABLET in 1 BOTTLE (68788-8425-3)
68788-8425-6	68788-8425	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230417	N/A	ANDA	ANDA077987	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	10 mg/1	60 TABLET in 1 BOTTLE (68788-8425-6)
68788-8425-9	68788-8425	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20230417	N/A	ANDA	ANDA077987	Preferred Pharmaceuticals Inc.	PRAVASTATIN SODIUM	10 mg/1	90 TABLET in 1 BOTTLE (68788-8425-9)
50090-5809-0	50090-5809	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20211015	N/A	ANDA	ANDA077987	A-S Medication Solutions	PRAVASTATIN SODIUM	80 mg/1	30 TABLET in 1 BOTTLE (50090-5809-0)
50090-5809-1	50090-5809	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20211015	N/A	ANDA	ANDA077987	A-S Medication Solutions	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (50090-5809-1)
60687-886-01	60687-886	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20250302	N/A	ANDA	ANDA077987	American Health Packaging	PRAVASTATIN SODIUM	10 mg/1	100 BLISTER PACK in 1 CARTON (60687-886-01) / 1 TABLET in 1 BLISTER PACK (60687-886-11)
16714-570-01	16714-570	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20220812	N/A	ANDA	ANDA077987	NorthStar RxLLC	PRAVASTATIN SODIUM	80 mg/1	90 TABLET in 1 BOTTLE (16714-570-01)
16714-570-02	16714-570	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20220812	N/A	ANDA	ANDA077987	NorthStar RxLLC	PRAVASTATIN SODIUM	80 mg/1	500 TABLET in 1 BOTTLE (16714-570-02)
60687-190-01	60687-190	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20170215	20260630	ANDA	ANDA077987	American Health Packaging	PRAVASTATIN SODIUM	40 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-190-01) / 1 TABLET in 1 BLISTER PACK (60687-190-11)
69097-788-05	69097-788	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240601	N/A	ANDA	ANDA077987	CIPLA USA INC.	PRAVASTATIN SODIUM	10 mg/1	90 TABLET in 1 BOTTLE (69097-788-05)
69097-788-12	69097-788	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240601	N/A	ANDA	ANDA077987	CIPLA USA INC.	PRAVASTATIN SODIUM	10 mg/1	500 TABLET in 1 BOTTLE (69097-788-12)
60687-908-01	60687-908	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20250302	N/A	ANDA	ANDA077987	American Health Packaging	PRAVASTATIN SODIUM	40 mg/1	100 BLISTER PACK in 1 CARTON (60687-908-01) / 1 TABLET in 1 BLISTER PACK (60687-908-11)
68462-196-05	68462-196	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20070511	N/A	ANDA	ANDA077987	Glenmark Pharmaceuticals Inc., USA	PRAVASTATIN SODIUM	20 mg/1	500 TABLET in 1 BOTTLE (68462-196-05)
68462-196-90	68462-196	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20070511	N/A	ANDA	ANDA077987	Glenmark Pharmaceuticals Inc., USA	PRAVASTATIN SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (68462-196-90)
60687-169-01	60687-169	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20161201	20260430	ANDA	ANDA077987	American Health Packaging	PRAVASTATIN SODIUM	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-169-01) / 1 TABLET in 1 BLISTER PACK (60687-169-11)
69097-791-05	69097-791	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240601	N/A	ANDA	ANDA077987	CIPLA USA INC.	PRAVASTATIN SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (69097-791-05)
69097-791-12	69097-791	HUMAN PRESCRIPTION DRUG	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	TABLET	ORAL	20240601	N/A	ANDA	ANDA077987	CIPLA USA INC.	PRAVASTATIN SODIUM	40 mg/1	500 TABLET in 1 BOTTLE (69097-791-12)
68462-198-05	68462-198	HUMAN PRESCRIPTION DRUG	Pravastatin Sodium	Pravastatin Sodium	TABLET	ORAL	20071228	N/A	ANDA	ANDA077987	Glenmark Pharmaceuticals Inc., USA	PRAVASTATIN SODIUM	80 mg/1	500 TABLET in 1 BOTTLE (68462-198-05)