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
62756-238-18	62756-238	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-238-18)
62756-238-86	62756-238	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62756-238-86)
62756-238-88	62756-238	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-238-88)
62756-239-18	62756-239	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-239-18)
62756-239-20	62756-239	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (62756-239-20)
62756-239-83	62756-239	HUMAN PRESCRIPTION DRUG	Capecitabine	Capecitabine	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA204668	Sun Pharmaceutical Industries, Inc.	CAPECITABINE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-239-83)