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
68788-9327-1	68788-9327	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150325	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	100 TABLET, COATED in 1 BOTTLE (68788-9327-1)
68788-9327-3	68788-9327	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150325	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, COATED in 1 BOTTLE (68788-9327-3)
68788-9327-6	68788-9327	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150325	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	60 TABLET, COATED in 1 BOTTLE (68788-9327-6)
68788-9313-9	68788-9313	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150325	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-9313-9)
51655-066-26	51655-066	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220711	N/A	ANDA	ANDA076118	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
51655-066-52	51655-066	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20160304	N/A	ANDA	ANDA076118	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)
68071-1770-1	68071-1770	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170802	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (68071-1770-1)
68788-9327-9	68788-9327	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150325	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-9327-9)
50090-3243-0	50090-3243	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171117	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE (50090-3243-0)
50090-3243-1	50090-3243	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171103	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-3243-1)
43063-679-30	43063-679	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20160609	N/A	ANDA	ANDA076118	PD-Rx Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30)
43063-679-90	43063-679	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20240607	N/A	ANDA	ANDA076118	PD-Rx Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)
68788-6889-1	68788-6889	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170206	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	100 TABLET, COATED in 1 BOTTLE (68788-6889-1)
68788-6889-3	68788-6889	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170206	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	30 TABLET, COATED in 1 BOTTLE (68788-6889-3)
68788-6889-6	68788-6889	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170206	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	60 TABLET, COATED in 1 BOTTLE (68788-6889-6)
68788-6889-8	68788-6889	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170206	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	120 TABLET, COATED in 1 BOTTLE (68788-6889-8)
68788-6889-9	68788-6889	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170206	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-6889-9)