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
82804-211-30	82804-211	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20250319	N/A	ANDA	ANDA078560	Proficient Rx LP	EZETIMIBE	10 mg/1	30 TABLET in 1 BOTTLE (82804-211-30)
50090-7338-0	50090-7338	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20241015	N/A	ANDA	ANDA078560	A-S Medication Solutions	EZETIMIBE	10 mg/1	90 TABLET in 1 BOTTLE (50090-7338-0)
68462-226-05	68462-226	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20220429	20270101	ANDA	ANDA078560	Glenmark Pharmaceuticals Inc., USA	EZETIMIBE	10 mg/1	500 TABLET in 1 BOTTLE (68462-226-05)
68462-226-10	68462-226	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20220429	20270101	ANDA	ANDA078560	Glenmark Pharmaceuticals Inc., USA	EZETIMIBE	10 mg/1	1000 TABLET in 1 BOTTLE (68462-226-10)
68462-226-11	68462-226	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20220429	20270101	ANDA	ANDA078560	Glenmark Pharmaceuticals Inc., USA	EZETIMIBE	10 mg/1	10 BLISTER PACK in 1 CARTON (68462-226-11) / 10 TABLET in 1 BLISTER PACK
68462-226-30	68462-226	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20220429	20270101	ANDA	ANDA078560	Glenmark Pharmaceuticals Inc., USA	EZETIMIBE	10 mg/1	30 TABLET in 1 BOTTLE (68462-226-30)
68462-226-90	68462-226	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20220429	20270101	ANDA	ANDA078560	Glenmark Pharmaceuticals Inc., USA	EZETIMIBE	10 mg/1	90 TABLET in 1 BOTTLE (68462-226-90)
50090-7339-0	50090-7339	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20241015	N/A	ANDA	ANDA078560	A-S Medication Solutions	EZETIMIBE	10 mg/1	30 TABLET in 1 BOTTLE (50090-7339-0)
50090-7339-1	50090-7339	HUMAN PRESCRIPTION DRUG	Ezetimibe	Ezetimibe	TABLET	ORAL	20241015	N/A	ANDA	ANDA078560	A-S Medication Solutions	EZETIMIBE	10 mg/1	90 TABLET in 1 BOTTLE (50090-7339-1)