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
65862-315-30	65862-315	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET, FILM COATED	ORAL	20090115	N/A	ANDA	ANDA078993	Aurobindo Pharma Limited	LEVETIRACETAM	1000 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-315-30)
65862-315-60	65862-315	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET, FILM COATED	ORAL	20090115	N/A	ANDA	ANDA078993	Aurobindo Pharma Limited	LEVETIRACETAM	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-315-60)
16571-788-50	16571-788	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET, FILM COATED	ORAL	20090115	20260331	ANDA	ANDA078993	Rising Pharma Holdings, Inc.	LEVETIRACETAM	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-788-50)
60687-657-01	60687-657	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET, FILM COATED	ORAL	20220804	N/A	ANDA	ANDA078993	American Health Packaging	LEVETIRACETAM	500 mg/1	100 BLISTER PACK in 1 CARTON (60687-657-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-657-11)
60687-668-01	60687-668	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET, FILM COATED	ORAL	20220804	N/A	ANDA	ANDA078993	American Health Packaging	LEVETIRACETAM	1000 mg/1	100 BLISTER PACK in 1 CARTON (60687-668-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-668-11)