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
82009-013-10	82009-013	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20220526	N/A	ANDA	ANDA200895	Quallent Pharmaceuticals Health LLC	SIMVASTATIN	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-013-10)
31722-512-01	31722-512	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA200895	Camber Pharmaceuticals, Inc.	SIMVASTATIN	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-512-01)
31722-512-10	31722-512	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA200895	Camber Pharmaceuticals, Inc.	SIMVASTATIN	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (31722-512-10)
31722-512-30	31722-512	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA200895	Camber Pharmaceuticals, Inc.	SIMVASTATIN	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-512-30)
31722-512-90	31722-512	HUMAN PRESCRIPTION DRUG	Simvastatin	Simvastatin	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA200895	Camber Pharmaceuticals, Inc.	SIMVASTATIN	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-512-90)