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
67184-0571-1	67184-0571	HUMAN PRESCRIPTION DRUG	Mirabegron	mirabegron	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250630	N/A	ANDA	ANDA217989	Qilu Pharmaceutical Co., Ltd.	MIRABEGRON	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67184-0571-1)
67184-0571-2	67184-0571	HUMAN PRESCRIPTION DRUG	Mirabegron	mirabegron	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250630	N/A	ANDA	ANDA217989	Qilu Pharmaceutical Co., Ltd.	MIRABEGRON	25 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67184-0571-2)
67184-0572-1	67184-0572	HUMAN PRESCRIPTION DRUG	Mirabgeorn	mirabegron	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250630	N/A	ANDA	ANDA217989	Qilu Pharmaceutical Co., Ltd.	MIRABEGRON	50 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67184-0572-1)
67184-0572-2	67184-0572	HUMAN PRESCRIPTION DRUG	Mirabgeorn	mirabegron	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250630	N/A	ANDA	ANDA217989	Qilu Pharmaceutical Co., Ltd.	MIRABEGRON	50 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67184-0572-2)