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
50242-923-01	50242-923	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20171116	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	150 mg/mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-923-01) / 1 mL in 1 VIAL, SINGLE-USE
50242-927-01	50242-927	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20240131	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	12 mg/.4mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-927-01) / .4 mL in 1 VIAL, SINGLE-USE
50242-930-01	50242-930	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20230316	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	300 mg/2mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-930-01) / 2 mL in 1 VIAL, SINGLE-USE
50242-922-01	50242-922	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20171116	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	105 mg/.7mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE
50242-921-01	50242-921	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20171116	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	60 mg/.4mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-921-01) / .4 mL in 1 VIAL, SINGLE-USE
50242-920-01	50242-920	HUMAN PRESCRIPTION DRUG	Hemlibra	emicizumab	INJECTION, SOLUTION	SUBCUTANEOUS	20171116	N/A	BLA	BLA761083	Genentech, Inc.	EMICIZUMAB	30 mg/mL	1 VIAL, SINGLE-USE in 1 CARTON (50242-920-01) / 1 mL in 1 VIAL, SINGLE-USE