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
68071-2813-9	68071-2813	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20220815	N/A	ANDA	ANDA202925	NuCare Pharmaceuticals,Inc.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2813-9)
50090-4918-0	50090-4918	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20200218	N/A	ANDA	ANDA202925	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4918-0)
50090-2598-1	50090-2598	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20161107	N/A	ANDA	ANDA202925	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-2598-1)
50090-2598-0	50090-2598	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20161104	N/A	ANDA	ANDA202925	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-2598-0)