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
50090-4275-0	50090-4275	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20190419	N/A	ANDA	ANDA091249	A-S Medication Solutions	MYCOPHENOLATE MOFETIL	500 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)
50268-558-15	50268-558	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20230515	N/A	ANDA	ANDA091249	AvPAK	MYCOPHENOLATE MOFETIL	500 mg/1	50 BLISTER PACK in 1 BOX (50268-558-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-558-11)
67877-225-01	67877-225	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20111128	N/A	ANDA	ANDA091249	Ascend Laboratories, LLC	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-225-01)
67877-225-05	67877-225	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20111128	N/A	ANDA	ANDA091249	Ascend Laboratories, LLC	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-225-05)
67877-225-38	67877-225	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20111128	N/A	ANDA	ANDA091249	Ascend Laboratories, LLC	MYCOPHENOLATE MOFETIL	500 mg/1	10 BLISTER PACK in 1 CARTON (67877-225-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
67877-225-84	67877-225	HUMAN PRESCRIPTION DRUG	Mycophenolate Mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20111128	N/A	ANDA	ANDA091249	Ascend Laboratories, LLC	MYCOPHENOLATE MOFETIL	500 mg/1	3 BLISTER PACK in 1 CARTON (67877-225-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK