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
67877-522-38	67877-522	HUMAN PRESCRIPTION DRUG	Ticagrelor	Ticagrelor	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA210219	Ascend Laboratories, LLC	TICAGRELOR	60 mg/1	10 BLISTER PACK in 1 CARTON (67877-522-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
67877-522-60	67877-522	HUMAN PRESCRIPTION DRUG	Ticagrelor	Ticagrelor	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA210219	Ascend Laboratories, LLC	TICAGRELOR	60 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (67877-522-60)
67877-522-18	67877-522	HUMAN PRESCRIPTION DRUG	Ticagrelor	Ticagrelor	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA210219	Ascend Laboratories, LLC	TICAGRELOR	60 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (67877-522-18)
67877-522-14	67877-522	HUMAN PRESCRIPTION DRUG	Ticagrelor	Ticagrelor	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA210219	Ascend Laboratories, LLC	TICAGRELOR	60 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (67877-522-14)
67877-522-05	67877-522	HUMAN PRESCRIPTION DRUG	Ticagrelor	Ticagrelor	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA210219	Ascend Laboratories, LLC	TICAGRELOR	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-522-05)