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
70771-1062-3	70771-1062	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA201686	Zydus Lifesciences Limited	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1062-3)
70771-1062-5	70771-1062	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA201686	Zydus Lifesciences Limited	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1062-5)
70771-1062-9	70771-1062	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA201686	Zydus Lifesciences Limited	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1062-9)
70771-1062-0	70771-1062	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20170208	N/A	ANDA	ANDA201686	Zydus Lifesciences Limited	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1062-0)
72578-012-10	72578-012	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA201686	Viona Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72578-012-10)
72578-012-06	72578-012	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA201686	Viona Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-012-06)
72578-012-05	72578-012	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA201686	Viona Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72578-012-05)
72578-012-16	72578-012	HUMAN PRESCRIPTION DRUG	clopidogrel	clopidogrel	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA201686	Viona Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72578-012-16)