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
71151-031-01	71151-031	HUMAN PRESCRIPTION DRUG	Mycophenolic Acid	Mycophenolic Acid	TABLET, DELAYED RELEASE	ORAL	20240105	N/A	ANDA	ANDA217031	airis PHARMA Private Limited	MYCOPHENOLATE SODIUM	360 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71151-031-01)
71151-030-01	71151-030	HUMAN PRESCRIPTION DRUG	Mycophenolic Acid	Mycophenolic Acid	TABLET, DELAYED RELEASE	ORAL	20240105	N/A	ANDA	ANDA217031	airis PHARMA Private Limited	MYCOPHENOLATE SODIUM	180 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71151-030-01)
70377-127-11	70377-127	HUMAN PRESCRIPTION DRUG	Mycophenolic Acid	Mycophenolic Acid	TABLET, DELAYED RELEASE	ORAL	20240930	N/A	ANDA	ANDA217031	Biocon Pharma Inc.	MYCOPHENOLATE SODIUM	360 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (70377-127-11)
70377-126-11	70377-126	HUMAN PRESCRIPTION DRUG	Mycophenolic Acid	Mycophenolic Acid	TABLET, DELAYED RELEASE	ORAL	20240930	N/A	ANDA	ANDA217031	Biocon Pharma Inc.	MYCOPHENOLATE SODIUM	180 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (70377-126-11)