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
0078-0690-61	0078-0690	HUMAN PRESCRIPTION DRUG	ARZERRA	ofatumumab	INJECTION, SOLUTION	INTRAVENOUS	20160201	N/A	BLA	BLA125326	Novartis Pharmaceuticals Corporation	OFATUMUMAB	20 mg/mL	50 mL in 1 VIAL, SINGLE-USE (0078-0690-61)
0078-0669-13	0078-0669	HUMAN PRESCRIPTION DRUG	ARZERRA	ofatumumab	INJECTION, SOLUTION	INTRAVENOUS	20160201	N/A	BLA	BLA125326	Novartis Pharmaceuticals Corporation	OFATUMUMAB	20 mg/mL	3 VIAL, SINGLE-USE in 1 CARTON (0078-0669-13) / 5 mL in 1 VIAL, SINGLE-USE (0078-0669-61)
0078-1007-68	0078-1007	HUMAN PRESCRIPTION DRUG	KESIMPTA	ofatumumab	INJECTION, SOLUTION	SUBCUTANEOUS	20200820	N/A	BLA	BLA125326	Novartis Pharmaceuticals Corporation	OFATUMUMAB	20 mg/.4mL	1 SYRINGE, GLASS in 1 CARTON (0078-1007-68) / .4 mL in 1 SYRINGE, GLASS
0078-1007-98	0078-1007	HUMAN PRESCRIPTION DRUG	KESIMPTA	ofatumumab	INJECTION, SOLUTION	SUBCUTANEOUS	20200820	N/A	BLA	BLA125326	Novartis Pharmaceuticals Corporation	OFATUMUMAB	20 mg/.4mL	1 SYRINGE, GLASS in 1 CARTON (0078-1007-98) / .4 mL in 1 SYRINGE, GLASS