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
71335-0548-0	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20210915	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-0548-0)
71335-0548-1	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180319	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0548-1)
71335-0548-2	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180305	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0548-2)
71335-0548-3	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180215	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0548-3)
71335-0548-4	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (71335-0548-4)
71335-0548-5	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-0548-5)
71335-0548-6	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180301	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0548-6)
71335-0548-7	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180423	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0548-7)
71335-0548-8	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0548-8)
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)
63187-059-30	63187-059	HUMAN PRESCRIPTION DRUG	TOPIRAMATE	TOPIRAMATE	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090278	Proficient Rx LP	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-059-30)
63187-059-90	63187-059	HUMAN PRESCRIPTION DRUG	TOPIRAMATE	TOPIRAMATE	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090278	Proficient Rx LP	TOPIRAMATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-059-90)
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)
47335-707-18	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)