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
72205-006-60	72205-006	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20180721	N/A	ANDA	ANDA209365	Novadoz Pharmaceuticals LLC	CAPECITABINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72205-006-60)
72205-007-92	72205-007	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20180721	N/A	ANDA	ANDA209365	Novadoz Pharmaceuticals LLC	CAPECITABINE	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (72205-007-92)
69097-949-03	69097-949	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20230701	N/A	ANDA	ANDA209365	Cipla USA Inc.	CAPECITABINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (69097-949-03)
69097-948-08	69097-948	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20230701	N/A	ANDA	ANDA209365	Cipla USA Inc.	CAPECITABINE	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (69097-948-08)