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
50228-124-10	50228-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (50228-124-10)
50228-124-30	50228-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50228-124-30)
50228-124-90	50228-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50228-124-90)
50228-121-30	50228-121	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50228-121-30)
50228-121-90	50228-121	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50228-121-90)
50228-124-05	50228-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20150915	N/A	ANDA	ANDA204165	ScieGen Pharmaceuticals Inc	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (50228-124-05)
50268-184-12	50268-184	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20191011	N/A	ANDA	ANDA204165	AvPAK	CLOPIDOGREL BISULFATE	300 mg/1	20 BLISTER PACK in 1 BOX (50268-184-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-184-11)
68071-5277-9	68071-5277	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA204165	NuCare Pharmaceuticals,Inc.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)
69367-194-05	69367-194	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20180727	N/A	ANDA	ANDA204165	Westminster Pharmaceuticals, LLC	CLOPIDOGREL BISULFATE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-05)
69367-194-30	69367-194	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20180727	N/A	ANDA	ANDA204165	Westminster Pharmaceuticals, LLC	CLOPIDOGREL BISULFATE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-30)
69367-200-05	69367-200	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel Bisulfate	TABLET, FILM COATED	ORAL	20230515	N/A	ANDA	ANDA204165	Westminster Pharmaceuticals, LLC	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-200-05)
72162-2212-0	72162-2212	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20240105	N/A	ANDA	ANDA204165	Bryant Ranch Prepack	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72162-2212-0)