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
43063-997-21	43063-997	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200421	N/A	ANDA	ANDA090278	PD-Rx Pharmaceuticals, Inc.	TOPIRAMATE	50 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-21)
43063-997-30	43063-997	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200823	N/A	ANDA	ANDA090278	PD-Rx Pharmaceuticals, Inc.	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-30)
43063-997-60	43063-997	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200718	N/A	ANDA	ANDA090278	PD-Rx Pharmaceuticals, Inc.	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-60)
43063-998-30	43063-998	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA090278	PD-Rx Pharmaceuticals, Inc.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-998-30)
43063-998-60	43063-998	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20190730	N/A	ANDA	ANDA090278	PD-Rx Pharmaceuticals, Inc.	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-998-60)
70518-0887-0	70518-0887	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20171204	N/A	ANDA	ANDA090278	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0887-0)