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=ANDA078462"
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
72789-443-60 72789-443 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA078462 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-443-60)
65862-171-99 65862-171 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-171-99)
65862-172-60 65862-172 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-172-60)
65862-172-99 65862-172 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-172-99)
65862-173-05 65862-173 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-173-05)
65862-173-60 65862-173 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-173-60)
65862-173-99 65862-173 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-173-99)
65862-174-05 65862-174 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-174-05)
65862-174-60 65862-174 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-174-60)
65862-174-99 65862-174 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-174-99)
65862-171-60 65862-171 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-171-60)
65862-171-05 65862-171 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-171-05)
65862-172-05 65862-172 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Aurobindo Pharma Limited TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-172-05)
16571-705-06 16571-705 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (16571-705-06)
16571-705-10 16571-705 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-705-10)
16571-707-06 16571-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (16571-707-06)
16571-708-06 16571-708 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (16571-708-06)
16571-708-10 16571-708 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-708-10)
80425-0202-2 80425-0202 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078462 Advanced Rx Pharmacy of Tennessee, LLC TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0202-2)
16571-707-10 16571-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA078462 Rising Pharma Holdings, Inc. TOPIRAMATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-707-10)
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