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
63187-362-30	63187-362	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA076999	Proficient Rx LP	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-362-30)
63187-362-60	63187-362	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA076999	Proficient Rx LP	CLOPIDOGREL BISULFATE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-362-60)
63187-362-90	63187-362	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA076999	Proficient Rx LP	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-362-90)
0093-7314-05	0093-7314	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA076999	Teva Pharmaceuticals USA, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-7314-05)
0093-7314-56	0093-7314	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA076999	Teva Pharmaceuticals USA, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7314-56)
0093-7314-98	0093-7314	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20120517	N/A	ANDA	ANDA076999	Teva Pharmaceuticals USA, Inc.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-7314-98)
68071-4138-3	68071-4138	HUMAN PRESCRIPTION DRUG	Clopidogrel	Clopidogrel	TABLET, FILM COATED	ORAL	20171031	N/A	ANDA	ANDA076999	NuCare Pharmaceuticals,Inc.	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)