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
62559-414-01	62559-414	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20221107	N/A	ANDA	ANDA076342	ANI Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET in 1 BOTTLE (62559-414-01)
62559-415-01	62559-415	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20221107	N/A	ANDA	ANDA076342	ANI Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (62559-415-01)
62559-416-01	62559-416	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20221107	N/A	ANDA	ANDA076342	ANI Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (62559-416-01)
62559-417-01	62559-417	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20221107	N/A	ANDA	ANDA076342	ANI Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (62559-417-01)