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
71205-202-30	71205-202	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-202-30)
71205-202-60	71205-202	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-202-60)
71205-202-90	71205-202	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-202-90)
71205-187-90	71205-187	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-187-90)
71205-195-60	71205-195	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-195-60)
71205-195-30	71205-195	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090162	Proficient Rx LP	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-195-30)
55700-995-30	55700-995	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230117	N/A	ANDA	ANDA090162	Quality Care Products, LLC	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-995-30)
55700-995-60	55700-995	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230117	N/A	ANDA	ANDA090162	Quality Care Products, LLC	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-995-60)