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
0955-1022-08	0955-1022	HUMAN PRESCRIPTION DRUG	Docetaxel	Docetaxel	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20161023	N/A	NDA AUTHORIZED GENERIC	NDA020449	Winthrop U.S, a business of sanofi-aventis U.S. LLC	DOCETAXEL	160 mg/8mL	1 VIAL, GLASS in 1 CARTON (0955-1022-08) / 8 mL in 1 VIAL, GLASS
0955-1021-04	0955-1021	HUMAN PRESCRIPTION DRUG	Docetaxel	Docetaxel	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20101021	N/A	NDA AUTHORIZED GENERIC	NDA020449	Winthrop U.S, a business of sanofi-aventis U.S. LLC	DOCETAXEL	80 mg/4mL	1 VIAL, GLASS in 1 CARTON (0955-1021-04) / 4 mL in 1 VIAL, GLASS
0955-1020-01	0955-1020	HUMAN PRESCRIPTION DRUG	Docetaxel	Docetaxel	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20101021	N/A	NDA AUTHORIZED GENERIC	NDA020449	Winthrop U.S, a business of sanofi-aventis U.S. LLC	DOCETAXEL	20 mg/mL	1 VIAL, GLASS in 1 CARTON (0955-1020-01) / 1 mL in 1 VIAL, GLASS