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
68788-7468-5 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5)
68788-7468-6 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6)
68788-7468-9 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)
50090-5853-0 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5853-0)
50090-5853-1 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5853-1)
50090-5853-2 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5853-2)
68382-141-01 68382-141 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-141-01)
68382-141-05 68382-141 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-141-05)
68382-141-14 68382-141 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68382-141-14)
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)
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)
80425-0092-2 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 60 TABLET, FILM COATED in 1 BOTTLE (80425-0092-2)
80425-0092-3 80425-0092 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240814 N/A ANDA ANDA078235 Advanced Rx Pharmacy of Tennessee, LLC TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0092-3)
82009-136-05 82009-136 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20230724 N/A ANDA ANDA078235 Quallent Pharmaceuticals Health LLC TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-136-05)
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)
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)
60760-075-30 60760-075 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20250820 N/A ANDA ANDA078235 ST. MARY'S MEDICAL PARK PHARMACY TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-075-30)
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