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
60505-4642-3	60505-4642	HUMAN PRESCRIPTION DRUG	PRASUGREL	PRASUGREL	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA205897	Apotex Corp.	PRASUGREL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-4642-3)
60505-4643-3	60505-4643	HUMAN PRESCRIPTION DRUG	PRASUGREL	PRASUGREL	TABLET, FILM COATED	ORAL	20171016	20270930	ANDA	ANDA205897	Apotex Corp.	PRASUGREL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-4643-3)
60505-4856-3	60505-4856	HUMAN PRESCRIPTION DRUG	PRASUGREL	PRASUGREL	TABLET, FILM COATED	ORAL	20250215	N/A	ANDA	ANDA205897	Apotex Corp.	PRASUGREL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-4856-3)
43817-239-01	43817-239	HUMAN PRESCRIPTION DRUG	PRASUGREL	PRASUGREL	TABLET, FILM COATED	ORAL	20171016	20270228	ANDA	ANDA205897	Panacea Biotec Limited	PRASUGREL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43817-239-01)
43817-240-01	43817-240	HUMAN PRESCRIPTION DRUG	PRASUGREL	PRASUGREL	TABLET, FILM COATED	ORAL	20171016	20261031	ANDA	ANDA205897	Panacea Biotec Limited	PRASUGREL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43817-240-01)