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
65162-871-10	65162-871	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20150529	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	4 mg/1	100 TABLET in 1 BOTTLE (65162-871-10)
65162-871-40	65162-871	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20210923	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	4 mg/1	1 BLISTER PACK in 1 CARTON (65162-871-40) / 21 TABLET in 1 BLISTER PACK
65162-984-29	65162-984	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20150529	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	32 mg/1	25 TABLET in 1 BOTTLE (65162-984-29)
65162-982-05	65162-982	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20150529	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	16 mg/1	50 TABLET in 1 BOTTLE (65162-982-05)
65162-982-29	65162-982	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20150529	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	16 mg/1	25 TABLET in 1 BOTTLE (65162-982-29)
65162-980-29	65162-980	HUMAN PRESCRIPTION DRUG	Methylprednisolone	Methylprednisolone	TABLET	ORAL	20150529	N/A	ANDA	ANDA207481	Amneal Pharmaceuticals LLC	METHYLPREDNISOLONE	8 mg/1	25 TABLET in 1 BOTTLE (65162-980-29)