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
0185-0277-01	0185-0277	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20040211	N/A	ANDA	ANDA076631	Sandoz Inc	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0185-0277-01)
0185-0236-01	0185-0236	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20150317	N/A	ANDA	ANDA076631	Sandoz Inc	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0185-0236-01)
0185-0211-01	0185-0211	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20040211	N/A	ANDA	ANDA076631	Sandoz Inc	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0185-0211-01)
0185-0325-01	0185-0325	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20140404	N/A	ANDA	ANDA076631	Sandoz Inc	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0185-0325-01)
68462-579-01	68462-579	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20231201	N/A	ANDA	ANDA076631	Glenmark Pharmaceuticals Inc., USA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-579-01)
68462-576-01	68462-576	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20231201	N/A	ANDA	ANDA076631	Glenmark Pharmaceuticals Inc., USA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-576-01)
68462-577-01	68462-577	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20231201	N/A	ANDA	ANDA076631	Glenmark Pharmaceuticals Inc., USA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-577-01)
68462-578-01	68462-578	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20231130	N/A	ANDA	ANDA076631	Glenmark Pharmaceuticals Inc., USA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-578-01)