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
0115-1722-01	0115-1722	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	5 mg/1	10 BLISTER PACK in 1 CARTON (0115-1722-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0115-1722-15)
0115-1722-03	0115-1722	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1722-03)
0115-1722-13	0115-1722	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1722-13)
0115-1721-01	0115-1721	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	2.5 mg/1	10 BLISTER PACK in 1 CARTON (0115-1721-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0115-1721-15)
0115-1721-03	0115-1721	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1721-03)
0115-1721-13	0115-1721	HUMAN PRESCRIPTION DRUG	Apixaban	Apixaban	TABLET, FILM COATED	ORAL	20180831	N/A	ANDA	ANDA209810	Amneal Pharmaceuticals of New York LLC	APIXABAN	2.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-1721-13)