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
62559-650-90	62559-650	HUMAN PRESCRIPTION DRUG	ATACAND HCT	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20181001	N/A	NDA	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	16 mg/1; 12.5 mg/1	90 TABLET in 1 BOTTLE (62559-650-90)
62559-651-90	62559-651	HUMAN PRESCRIPTION DRUG	ATACAND HCT	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20181001	N/A	NDA	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	32 mg/1; 12.5 mg/1	90 TABLET in 1 BOTTLE (62559-651-90)
62559-652-90	62559-652	HUMAN PRESCRIPTION DRUG	ATACAND HCT	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20181001	N/A	NDA	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	32 mg/1; 25 mg/1	90 TABLET in 1 BOTTLE (62559-652-90)
62559-660-90	62559-660	HUMAN PRESCRIPTION DRUG	Candesartan Cilexetil and Hydrochlorothiazide	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20180926	N/A	NDA AUTHORIZED GENERIC	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	16 mg/1; 12.5 mg/1	90 TABLET in 1 BOTTLE (62559-660-90)
62559-661-90	62559-661	HUMAN PRESCRIPTION DRUG	Candesartan Cilexetil and Hydrochlorothiazide	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20180926	N/A	NDA AUTHORIZED GENERIC	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	32 mg/1; 12.5 mg/1	90 TABLET in 1 BOTTLE (62559-661-90)
62559-662-90	62559-662	HUMAN PRESCRIPTION DRUG	Candesartan Cilexetil and Hydrochlorothiazide	Candesartan Cilexetil and Hydrochlorothiazide	TABLET	ORAL	20180926	N/A	NDA AUTHORIZED GENERIC	NDA021093	ANI Pharmaceuticals, Inc.	CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE	32 mg/1; 25 mg/1	90 TABLET in 1 BOTTLE (62559-662-90)