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
70377-005-13	70377-005	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20151217	N/A	ANDA	ANDA078034	Biocon Pharma Inc,	SIMVASTATIN	80 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (70377-005-13)
70377-005-14	70377-005	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20151217	N/A	ANDA	ANDA078034	Biocon Pharma Inc,	SIMVASTATIN	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70377-005-14)
70377-005-15	70377-005	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20151217	N/A	ANDA	ANDA078034	Biocon Pharma Inc,	SIMVASTATIN	80 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70377-005-15)
51655-113-26	51655-113	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA078034	Northwind Pharmaceuticals, LLC	SIMVASTATIN	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-113-26)
51655-113-52	51655-113	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20231226	N/A	ANDA	ANDA078034	Northwind Pharmaceuticals, LLC	SIMVASTATIN	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-113-52)
51655-448-26	51655-448	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20201013	N/A	ANDA	ANDA078034	Northwind Pharmaceuticals, LLC	SIMVASTATIN	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-448-26)
51655-448-52	51655-448	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20230222	N/A	ANDA	ANDA078034	Northwind Pharmaceuticals, LLC	SIMVASTATIN	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-448-52)
50090-6459-0	50090-6459	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20230501	N/A	ANDA	ANDA078034	A-S Medication Solutions	SIMVASTATIN	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6459-0)