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
65862-357-01	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-357-01)
65862-357-05	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-357-05)
65862-357-10	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	10 BLISTER PACK in 1 CARTON (65862-357-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-357-30	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-357-30)
65862-357-90	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-357-90)
65862-357-99	65862-357	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA090540	Aurobindo Pharma Limited	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-357-99)