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
61919-823-30	61919-823	HUMAN PRESCRIPTION DRUG	TOPIRAMATE	TOPIRAMATE	TABLET, FILM COATED	ORAL	20150101	N/A	ANDA	ANDA090278	DirectRX	TOPIRAMATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (61919-823-30)
61919-823-60	61919-823	HUMAN PRESCRIPTION DRUG	TOPIRAMATE	TOPIRAMATE	TABLET, FILM COATED	ORAL	20150101	N/A	ANDA	ANDA090278	DirectRX	TOPIRAMATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (61919-823-60)
47335-711-08	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-711-08)
47335-711-13	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-711-13)
47335-711-18	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-711-18)
47335-711-83	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-711-83)
47335-711-86	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-711-86)
47335-711-88	47335-711	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-711-88)
47335-710-08	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-710-08)
47335-710-13	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-710-13)
47335-710-18	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-710-18)
47335-710-83	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-710-83)
47335-710-86	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-710-86)
47335-710-88	47335-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-710-88)
62756-710-08	62756-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-710-08)
62756-710-13	62756-710	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-710-13)
61919-824-90	61919-824	HUMAN PRESCRIPTION DRUG	TOPIRAMATE	TOPIRAMATE	TABLET, FILM COATED	ORAL	20140328	N/A	ANDA	ANDA090278	DIRECT RX	TOPIRAMATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (61919-824-90)
47335-712-08	47335-712	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-712-08)
47335-712-13	47335-712	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-712-13)
47335-712-18	47335-712	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18)