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)
检索条件:" 注册申请号=ANDA078235"
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
65841-647-01 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-647-01)
65841-647-05 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-647-05)
65841-647-14 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65841-647-14)
65841-647-16 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-647-16)
70518-1937-0 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1937-0)
0904-6929-61 0904-6929 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Major Pharmaceuticals TOPIRAMATE 100 mg/1 100 BLISTER PACK in 1 CARTON (0904-6929-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
65841-648-01 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-648-01)
65841-648-05 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-648-05)
65841-648-14 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65841-648-14)
65841-648-16 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-648-16)
70518-1953-0 70518-1953 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190313 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1953-0)
70518-1953-1 70518-1953 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191016 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1953-1)
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)
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)
80425-0092-1 80425-0092 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Advanced Rx Pharmacy of Tennessee, LLC TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0092-1)
82009-137-05 82009-137 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20230724 N/A ANDA ANDA078235 Quallent Pharmaceuticals Health LLC TOPIRAMATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-137-05)
68382-139-01 68382-139 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-139-01)
68382-139-05 68382-139 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-139-05)
68382-139-14 68382-139 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68382-139-14)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase