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
30698-452-01	30698-452	HUMAN PRESCRIPTION DRUG	Lotensin HCT	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	19920530	N/A	NDA	NDA020033	Validus Pharmaceuticals LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (30698-452-01)
30698-453-01	30698-453	HUMAN PRESCRIPTION DRUG	Lotensin HCT	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	19920530	N/A	NDA	NDA020033	Validus Pharmaceuticals LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (30698-453-01)
30698-454-01	30698-454	HUMAN PRESCRIPTION DRUG	Lotensin HCT	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	19920530	N/A	NDA	NDA020033	Validus Pharmaceuticals LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (30698-454-01)
0574-0227-01	0574-0227	HUMAN PRESCRIPTION DRUG	benazepril hydrochloride and hydrochlorothiazide	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	20190407	N/A	NDA AUTHORIZED GENERIC	NDA020033	Padagis US LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (0574-0227-01)
0574-0228-01	0574-0228	HUMAN PRESCRIPTION DRUG	benazepril hydrochloride and hydrochlorothiazide	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	20190407	N/A	NDA AUTHORIZED GENERIC	NDA020033	Padagis US LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (0574-0228-01)
0574-0229-01	0574-0229	HUMAN PRESCRIPTION DRUG	benazepril hydrochloride and hydrochlorothiazide	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	20190407	N/A	NDA AUTHORIZED GENERIC	NDA020033	Padagis US LLC	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (0574-0229-01)
72162-2328-1	72162-2328	HUMAN PRESCRIPTION DRUG	benazepril hydrochloride and hydrochlorothiazide	benazepril hydrochloride and hydrochlorothiazide	TABLET	ORAL	20240618	N/A	NDA AUTHORIZED GENERIC	NDA020033	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (72162-2328-1)