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
47335-894-81	47335-894	HUMAN PRESCRIPTION DRUG	Clopidogrel Bisulfate	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120518	N/A	ANDA	ANDA090494	Sun Pharmaceutical Industries, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (47335-894-81)
47335-894-83	47335-894	HUMAN PRESCRIPTION DRUG	Clopidogrel Bisulfate	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120518	N/A	ANDA	ANDA090494	Sun Pharmaceutical Industries, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-894-83)
47335-894-19	47335-894	HUMAN PRESCRIPTION DRUG	Clopidogrel Bisulfate	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120518	N/A	ANDA	ANDA090494	Sun Pharmaceutical Industries, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (47335-894-19)
47335-894-18	47335-894	HUMAN PRESCRIPTION DRUG	Clopidogrel Bisulfate	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120518	N/A	ANDA	ANDA090494	Sun Pharmaceutical Industries, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-894-18)
47335-894-13	47335-894	HUMAN PRESCRIPTION DRUG	Clopidogrel Bisulfate	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20120518	N/A	ANDA	ANDA090494	Sun Pharmaceutical Industries, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-894-13)