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
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)
71335-0325-1	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181127	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0325-1)
71335-0325-2	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181228	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0325-2)
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)
47335-712-83	47335-712	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-712-83)
47335-712-86	47335-712	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-712-86)
47335-712-88	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 (47335-712-88)
71335-0487-0	71335-0487	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0487-0)
71335-0487-1	71335-0487	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181204	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0487-1)
47335-707-08	47335-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-707-08)
47335-707-13	47335-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-707-13)
47335-707-18	47335-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-707-18)
47335-707-83	47335-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA090278	Sun Pharmaceutical Industries, Inc.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-707-83)