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
0781-5175-01	0781-5175	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20081015	N/A	ANDA	ANDA065451	Sandoz Inc	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5175-01)
0781-5175-05	0781-5175	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20081015	N/A	ANDA	ANDA065451	Sandoz Inc	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0781-5175-05)
0781-5175-10	0781-5175	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20081015	N/A	ANDA	ANDA065451	Sandoz Inc	MYCOPHENOLATE MOFETIL	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)
0480-3571-01	0480-3571	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA065451	Teva Pharmaceuticals USA, Inc.	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0480-3571-01)
0480-3571-05	0480-3571	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA065451	Teva Pharmaceuticals USA, Inc.	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0480-3571-05)