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=ANDA084612"
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
63629-3742-7 63629-3742 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20080707 N/A ANDA ANDA084612 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 28 TABLET in 1 BOTTLE (63629-3742-7)
63629-3742-8 63629-3742 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20080707 N/A ANDA ANDA084612 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 90 TABLET in 1 BOTTLE (63629-3742-8)
63629-3742-9 63629-3742 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20080707 N/A ANDA ANDA084612 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 10 TABLET in 1 BOTTLE (63629-3742-9)
69306-114-06 69306-114 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20201008 N/A ANDA ANDA084612 Doc Rx DEXAMETHASONE 4 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (69306-114-06)
69306-114-30 69306-114 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20200701 N/A ANDA ANDA084612 Doc Rx DEXAMETHASONE 4 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (69306-114-30)
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