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=ANDA040635"
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
0832-0512-00 0832-0512 HUMAN PRESCRIPTION DRUG Bethanechol Chloride Bethanechol Chloride TABLET ORAL 20100124 N/A ANDA ANDA040635 Upsher-Smith Laboratories, LLC BETHANECHOL CHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (0832-0512-00)
0832-0512-01 0832-0512 HUMAN PRESCRIPTION DRUG Bethanechol Chloride Bethanechol Chloride TABLET ORAL 20100124 N/A ANDA ANDA040635 Upsher-Smith Laboratories, LLC BETHANECHOL CHLORIDE 25 mg/1 100 BLISTER PACK in 1 CARTON (0832-0512-01) / 1 TABLET in 1 BLISTER PACK (0832-0512-89)
0832-0512-10 0832-0512 HUMAN PRESCRIPTION DRUG Bethanechol Chloride Bethanechol Chloride TABLET ORAL 20100124 N/A ANDA ANDA040635 Upsher-Smith Laboratories, LLC BETHANECHOL CHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (0832-0512-10)
0832-0512-25 0832-0512 HUMAN PRESCRIPTION DRUG Bethanechol Chloride Bethanechol Chloride TABLET ORAL 20100124 N/A ANDA ANDA040635 Upsher-Smith Laboratories, LLC BETHANECHOL CHLORIDE 25 mg/1 250 TABLET in 1 BOTTLE (0832-0512-25)
0832-0512-50 0832-0512 HUMAN PRESCRIPTION DRUG Bethanechol Chloride Bethanechol Chloride TABLET ORAL 20100124 N/A ANDA ANDA040635 Upsher-Smith Laboratories, LLC BETHANECHOL CHLORIDE 25 mg/1 500 TABLET in 1 BOTTLE (0832-0512-50)
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