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
72572-035-10	72572-035	HUMAN PRESCRIPTION DRUG	bivalirudin	bivalirudin	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20201221	N/A	NDA AUTHORIZED GENERIC	NDA020873	Civica, Inc.	BIVALIRUDIN	250 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (72572-035-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (72572-035-01)
0781-3158-95	0781-3158	HUMAN PRESCRIPTION DRUG	bivalirudin	bivalirudin	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20150615	N/A	NDA AUTHORIZED GENERIC	NDA020873	Sandoz Inc	BIVALIRUDIN	250 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (0781-3158-95) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (0781-3158-94)
0781-3447-95	0781-3447	HUMAN PRESCRIPTION DRUG	Angiomax	bivalirudin	INJECTION	INTRAVENOUS	20190801	N/A	NDA	NDA020873	Sandoz Inc	BIVALIRUDIN	250 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (0781-3447-95) / 1 INJECTION in 1 VIAL, SINGLE-USE
0781-9158-95	0781-9158	HUMAN PRESCRIPTION DRUG	bivalirudin	bivalirudin	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20151023	N/A	NDA AUTHORIZED GENERIC	NDA020873	Sandoz Inc	BIVALIRUDIN	250 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (0781-9158-95) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (0781-9158-94)
75929-217-01	75929-217	HUMAN PRESCRIPTION DRUG	bivalirudin	bivalirudin	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20201221	N/A	NDA AUTHORIZED GENERIC	NDA020873	Pharma Packaging Solutions, LLC dba Tjoapack LLC	BIVALIRUDIN	250 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (75929-217-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE