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
50242-135-01	50242-135	HUMAN PRESCRIPTION DRUG	ACTEMRA	tocilizumab	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20100108	N/A	BLA	BLA125276	Genentech, Inc.	TOCILIZUMAB	80 mg/4mL	1 VIAL, SINGLE-USE in 1 BOX (50242-135-01) / 4 mL in 1 VIAL, SINGLE-USE
50242-136-01	50242-136	HUMAN PRESCRIPTION DRUG	ACTEMRA	tocilizumab	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20100108	N/A	BLA	BLA125276	Genentech, Inc.	TOCILIZUMAB	200 mg/10mL	1 VIAL, SINGLE-USE in 1 BOX (50242-136-01) / 10 mL in 1 VIAL, SINGLE-USE
50242-137-01	50242-137	HUMAN PRESCRIPTION DRUG	ACTEMRA	tocilizumab	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20100108	N/A	BLA	BLA125276	Genentech, Inc.	TOCILIZUMAB	400 mg/20mL	1 VIAL, SINGLE-USE in 1 BOX (50242-137-01) / 20 mL in 1 VIAL, SINGLE-USE