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
70518-3758-0	70518-3758	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20230611	N/A	ANDA	ANDA078462	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3758-0)
16571-705-06	16571-705	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-705-06)
16571-705-10	16571-705	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-705-10)
16571-706-06	16571-706	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-706-06)
16571-706-10	16571-706	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-706-10)
16571-707-06	16571-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-707-06)
16571-707-10	16571-707	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-707-10)
16571-708-06	16571-708	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (16571-708-06)
16571-708-10	16571-708	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Rising Pharma Holdings, Inc.	TOPIRAMATE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-708-10)
65862-171-05	65862-171	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-171-05)
65862-171-60	65862-171	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-171-60)
65862-171-99	65862-171	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-171-99)
65862-172-05	65862-172	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-172-05)
65862-172-60	65862-172	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-172-60)
65862-172-99	65862-172	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-172-99)
65862-173-05	65862-173	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-173-05)
65862-173-60	65862-173	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-173-60)
65862-173-99	65862-173	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-173-99)
65862-174-05	65862-174	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220411	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-174-05)
65862-174-60	65862-174	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078462	Aurobindo Pharma Limited	TOPIRAMATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-174-60)