产品NDC51672-4106
产品类型HUMAN PRESCRIPTION DRUG
商品名Oxcarbazepine
商品名后缀
通用名Oxcarbazepine
剂型TABLET
给药途径ORAL
上市日期20071115
中止上市日期
市场分类ANDA
申请号ANDA077801
标签持有者Taro Pharmaceuticals U.S.A., Inc.
活性成分OXCARBAZEPINE
规格300
规格单位mg/1
药学分类Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA N 20211231
药品包装规格及说明书信息
产品NDC NDC包装代码 包装描述 药品说明书
51672-410651672-4106-010 BLISTER PACK in 1 CARTON (51672-4106-0) > 10 TABLET in 1 BLISTER PACK 20071115 N N药品说明书及标签信息
51672-410651672-4106-1100 TABLET in 1 BOTTLE (51672-4106-1) 20071115 N N药品说明书及标签信息
51672-410651672-4106-31000 TABLET in 1 BOTTLE (51672-4106-3) 20071115 N N药品说明书及标签信息
51672-410651672-4106-630 TABLET in 1 BOTTLE (51672-4106-6) 20071115 N N药品说明书及标签信息