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
65862-830-30	65862-830	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA205888	Aurobindo Pharma Limited	PRASUGREL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-830-30)
65862-830-03	65862-830	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA205888	Aurobindo Pharma Limited	PRASUGREL HYDROCHLORIDE	10 mg/1	3 BLISTER PACK in 1 CARTON (65862-830-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-830-10)
65862-829-30	65862-829	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA205888	Aurobindo Pharma Limited	PRASUGREL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-829-30)
65862-829-03	65862-829	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA205888	Aurobindo Pharma Limited	PRASUGREL HYDROCHLORIDE	5 mg/1	3 BLISTER PACK in 1 CARTON (65862-829-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-829-10)
60687-883-21	60687-883	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20250302	N/A	ANDA	ANDA205888	American Health Packaging	PRASUGREL HYDROCHLORIDE	10 mg/1	30 BLISTER PACK in 1 CARTON (60687-883-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-883-11)
63629-4829-1	63629-4829	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20241125	N/A	ANDA	ANDA205888	Bryant Ranch Prepack	PRASUGREL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-4829-1)
63629-4829-2	63629-4829	HUMAN PRESCRIPTION DRUG	Prasugrel	Prasugrel	TABLET, FILM COATED	ORAL	20241125	N/A	ANDA	ANDA205888	Bryant Ranch Prepack	PRASUGREL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-4829-2)