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
60760-352-90	60760-352	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171115	N/A	ANDA	ANDA076118	St. Mary's Medical Park Pharmacy	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-352-90)
60760-351-90	60760-351	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171115	N/A	ANDA	ANDA076118	St. Mary's Medical Park Pharmacy	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-351-90)
43063-677-90	43063-677	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20240607	N/A	ANDA	ANDA076118	PD-Rx Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-90)
43063-677-30	43063-677	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20160609	N/A	ANDA	ANDA076118	PD-Rx Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-30)
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	20230118	N/A	ANDA	ANDA076118	PD-Rx Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)
68071-3057-2	68071-3057	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20180802	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	120 TABLET, COATED in 1 BOTTLE (68071-3057-2)
68071-3057-3	68071-3057	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20180802	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, COATED in 1 BOTTLE (68071-3057-3)
68071-3057-6	68071-3057	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20180802	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	60 TABLET, COATED in 1 BOTTLE (68071-3057-6)
68071-3057-9	68071-3057	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20180802	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE (68071-3057-9)
68071-3324-1	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	120 TABLET, COATED in 1 BOTTLE (68071-3324-1)
68071-3324-3	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	30 TABLET, COATED in 1 BOTTLE (68071-3324-3)
68071-3324-6	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	60 TABLET, COATED in 1 BOTTLE (68071-3324-6)
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)
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)
68788-6889-1	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)
68788-6957-3	68788-6957	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170502	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (68788-6957-3)
68788-6957-9	68788-6957	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170502	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-6957-9)