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
67877-718-31	67877-718	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20211127	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.25 mg/1	6 BLISTER PACK in 1 CARTON (67877-718-31) / 10 TABLET in 1 BLISTER PACK (67877-718-33)
67877-718-60	67877-718	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20240301	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.25 mg/1	60 TABLET in 1 BOTTLE (67877-718-60)
67877-719-31	67877-719	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20211127	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.5 mg/1	6 BLISTER PACK in 1 CARTON (67877-719-31) / 10 TABLET in 1 BLISTER PACK (67877-719-33)
67877-719-60	67877-719	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20240301	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.5 mg/1	60 TABLET in 1 BOTTLE (67877-719-60)
67877-720-31	67877-720	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20211127	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.75 mg/1	6 BLISTER PACK in 1 CARTON (67877-720-31) / 10 TABLET in 1 BLISTER PACK (67877-720-33)
67877-720-60	67877-720	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20240301	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	.75 mg/1	60 TABLET in 1 BOTTLE (67877-720-60)
67877-721-31	67877-721	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20211127	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	1 mg/1	6 BLISTER PACK in 1 CARTON (67877-721-31) / 10 TABLET in 1 BLISTER PACK (67877-721-33)
67877-721-60	67877-721	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20211127	N/A	ANDA	ANDA214138	Ascend Laboratories, LLC	EVEROLIMUS	1 mg/1	60 TABLET in 1 BOTTLE (67877-721-60)