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
70771-1149-0	70771-1149	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1149-0)
70771-1149-1	70771-1149	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1149-1)
70771-1149-4	70771-1149	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	100 BLISTER PACK in 1 CARTON (70771-1149-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1149-2)
70771-1149-9	70771-1149	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1149-9)
70771-1150-0	70771-1150	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1150-0)
70771-1150-1	70771-1150	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1150-1)
70771-1150-4	70771-1150	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 CARTON (70771-1150-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1150-2)
70771-1150-9	70771-1150	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1150-9)
70771-1151-0	70771-1151	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1151-0)
70771-1151-1	70771-1151	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1151-1)
70771-1151-4	70771-1151	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 BLISTER PACK in 1 CARTON (70771-1151-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1151-2)
70771-1151-9	70771-1151	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1151-9)
70771-1148-9	70771-1148	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1148-9)
70771-1148-1	70771-1148	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1148-1)
70771-1148-0	70771-1148	HUMAN PRESCRIPTION DRUG	Benazepril hydrochloride	Benazepril hydrochloride	TABLET, FILM COATED	ORAL	20171113	N/A	ANDA	ANDA078848	Zydus Lifesciences Limited	BENAZEPRIL HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1148-0)