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)
产品NDC51672-4107
产品类型HUMAN PRESCRIPTION DRUG
商品名Oxcarbazepine
通用名Oxcarbazepine
剂型TABLET
给药途径ORAL
市场类别ANDA
申请号ANDA077801
标签持有者Taro Pharmaceuticals U.S.A., Inc.
活性成分OXCARBAZEPINE
规格600 mg/1
药学分类Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA计划编号N/A
上市认证有效期20241231
<<-药品包装规格及说明书信息->>
产品NDCNDC包装代码包装描述开始上市日期结束上市日期NDC号状态是否样品包装药品说明书
51672-410751672-4107-010 BLISTER PACK in 1 CARTON (51672-4107-0) / 10 TABLET in 1 BLISTER PACK20071115有效药品说明书及标签信息
51672-410751672-4107-1100 TABLET in 1 BOTTLE (51672-4107-1) 20071115有效药品说明书及标签信息
51672-410751672-4107-31000 TABLET in 1 BOTTLE (51672-4107-3) 20071115有效药品说明书及标签信息
51672-410751672-4107-630 TABLET in 1 BOTTLE (51672-4107-6) 20071115有效药品说明书及标签信息
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase