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
42543-713-01	42543-713	HUMAN PRESCRIPTION DRUG	Clopidogrel	clopidogrel	TABLET	ORAL	20141101	N/A	ANDA	ANDA204165	Vensun Pharmaceuticals, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	100 TABLET in 1 BOTTLE (42543-713-01)
77771-121-05	77771-121	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (77771-121-05)
77771-124-30	77771-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (77771-124-30)
77771-124-90	77771-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (77771-124-90)
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)
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)
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)
77771-121-30	77771-121	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (77771-121-30)
77771-121-90	77771-121	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (77771-121-90)
77771-124-10	77771-124	HUMAN PRESCRIPTION DRUG	Clopidogrel bisulfate	Clopidogrel bisulfate	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA204165	RADHA PHARMACEUTICALS, INC.	CLOPIDOGREL BISULFATE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (77771-124-10)
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)