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
68462-682-01	68462-682	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20201016	N/A	ANDA	ANDA208691	Glenmark Pharmaceuticals Inc., USA	SIROLIMUS	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-682-01)
68462-683-01	68462-683	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20201016	N/A	ANDA	ANDA208691	Glenmark Pharmaceuticals Inc., USA	SIROLIMUS	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-683-01)
68462-684-01	68462-684	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20201016	N/A	ANDA	ANDA208691	Glenmark Pharmaceuticals Inc., USA	SIROLIMUS	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-684-01)
16714-189-01	16714-189	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA208691	NORTHSTAR RX LLC	SIROLIMUS	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-189-01)
16714-188-01	16714-188	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA208691	NORTHSTAR RX LLC	SIROLIMUS	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-188-01)
16714-187-01	16714-187	HUMAN PRESCRIPTION DRUG	sirolimus	sirolimus	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA208691	NORTHSTAR RX LLC	SIROLIMUS	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-187-01)