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
69102-106-01	69102-106	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20201028	N/A	ANDA	ANDA078858	OWP Pharmaceuticals, Inc.	LEVETIRACETAM	750 mg/1	120 TABLET in 1 BOTTLE (69102-106-01)
13668-016-05	13668-016	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20090115	N/A	ANDA	ANDA078858	Torrent Pharmaceuticals Limited	LEVETIRACETAM	750 mg/1	500 TABLET in 1 BOTTLE (13668-016-05)
13668-016-12	13668-016	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20090115	N/A	ANDA	ANDA078858	Torrent Pharmaceuticals Limited	LEVETIRACETAM	750 mg/1	120 TABLET in 1 BOTTLE (13668-016-12)
13668-016-25	13668-016	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20090115	N/A	ANDA	ANDA078858	Torrent Pharmaceuticals Limited	LEVETIRACETAM	750 mg/1	250 TABLET in 1 BOTTLE (13668-016-25)
13668-016-60	13668-016	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20090115	N/A	ANDA	ANDA078858	Torrent Pharmaceuticals Limited	LEVETIRACETAM	750 mg/1	60 TABLET in 1 BOTTLE (13668-016-60)
13668-016-67	13668-016	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20090115	N/A	ANDA	ANDA078858	Torrent Pharmaceuticals Limited	LEVETIRACETAM	750 mg/1	800 TABLET in 1 BOTTLE (13668-016-67)
71335-2282-1	71335-2282	HUMAN PRESCRIPTION DRUG	Levetiracetam	Levetiracetam	TABLET	ORAL	20240812	N/A	ANDA	ANDA078858	Bryant Ranch Prepack	LEVETIRACETAM	500 mg/1	500 TABLET in 1 BOTTLE (71335-2282-1)