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
68001-541-36	68001-541	HUMAN PRESCRIPTION DRUG	Bortezomib	Bortezomib	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20220731	N/A	ANDA	ANDA209622	BluePoint Laboratories	BORTEZOMIB	3.5 mg/3.5mL	1 VIAL, SINGLE-USE in 1 CARTON (68001-541-36) / 3.5 mL in 1 VIAL, SINGLE-USE
72205-183-01	72205-183	HUMAN PRESCRIPTION DRUG	Bortezomib	Bortezomib	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20220727	N/A	ANDA	ANDA209622	Novadoz Pharmaceuticals LLC	BORTEZOMIB	3.5 mg/3.5mL	1 VIAL, SINGLE-USE in 1 CARTON (72205-183-01) / 3.5 mL in 1 VIAL, SINGLE-USE
83090-008-01	83090-008	HUMAN PRESCRIPTION DRUG	Bortezomib	Bortezomib	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20230715	N/A	ANDA	ANDA209622	Sintetica US LLC	BORTEZOMIB	3.5 mg/3.5mL	1 VIAL, SINGLE-DOSE in 1 CARTON (83090-008-01) / 3.5 mL in 1 VIAL, SINGLE-DOSE