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
51655-429-26	51655-429	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230324	N/A	ANDA	ANDA078235	Northwind Pharmaceuticals, LLC	TOPIRAMATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-429-26)
51655-746-26	51655-746	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230105	N/A	ANDA	ANDA078235	Northwind Pharmaceuticals, LLC	TOPIRAMATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-26)
51655-746-52	51655-746	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20221230	N/A	ANDA	ANDA078235	Northwind Pharmaceuticals, LLC	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-52)
51655-848-26	51655-848	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230417	N/A	ANDA	ANDA078235	Northwind Pharmaceuticals, LLC	TOPIRAMATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-848-26)
65841-650-01	65841-650	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Zydus Lifesciences Limited	TOPIRAMATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-650-01)
65841-650-05	65841-650	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Zydus Lifesciences Limited	TOPIRAMATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-650-05)
65841-650-14	65841-650	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Zydus Lifesciences Limited	TOPIRAMATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65841-650-14)
65841-650-16	65841-650	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Zydus Lifesciences Limited	TOPIRAMATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-650-16)
51655-848-52	51655-848	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230206	N/A	ANDA	ANDA078235	Northwind Pharmaceuticals, LLC	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-848-52)
55154-7142-0	55154-7142	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20120601	N/A	ANDA	ANDA078235	Cardinal Health 107, LLC	TOPIRAMATE	100 mg/1	10 BLISTER PACK in 1 BAG (55154-7142-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68084-342-01	68084-342	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090410	N/A	ANDA	ANDA078235	American Health Packaging	TOPIRAMATE	25 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-342-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-342-11)
68084-345-21	68084-345	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090413	N/A	ANDA	ANDA078235	American Health Packaging	TOPIRAMATE	200 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-345-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-345-11)
55154-7146-0	55154-7146	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20120601	N/A	ANDA	ANDA078235	Cardinal Health 107, LLC	TOPIRAMATE	25 mg/1	10 BLISTER PACK in 1 BAG (55154-7146-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-0233-0	70518-0233	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20170216	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0233-0)
68084-343-01	68084-343	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20191108	N/A	ANDA	ANDA078235	American Health Packaging	TOPIRAMATE	50 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-343-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-343-11)
70518-1718-1	70518-1718	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20200211	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	30 POUCH in 1 BOX (70518-1718-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1718-2)
70518-1718-3	70518-1718	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20210526	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1718-3)
70518-1718-4	70518-1718	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1718-4)
68084-344-01	68084-344	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090421	N/A	ANDA	ANDA078235	American Health Packaging	TOPIRAMATE	100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-344-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-344-11)
70518-1718-0	70518-1718	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20181207	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1718-0)