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=ANDA203374"
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
50228-109-30 50228-109 HUMAN PRESCRIPTION DRUG CARISOPRODOL CARISOPRODOL TABLET ORAL 20140127 N/A ANDA ANDA203374 ScieGen Pharmaceuticals, Inc. CARISOPRODOL 350 mg/1 30 TABLET in 1 BOTTLE (50228-109-30)
42543-700-01 42543-700 HUMAN PRESCRIPTION DRUG CARISOPRODOL CARISOPRODOL TABLET ORAL 20140731 N/A ANDA ANDA203374 Vensun Pharmaceuticals, Inc. CARISOPRODOL 350 mg/1 100 TABLET in 1 BOTTLE (42543-700-01)
42543-700-05 42543-700 HUMAN PRESCRIPTION DRUG CARISOPRODOL CARISOPRODOL TABLET ORAL 20140731 N/A ANDA ANDA203374 Vensun Pharmaceuticals, Inc. CARISOPRODOL 350 mg/1 500 TABLET in 1 BOTTLE (42543-700-05)
42543-700-10 42543-700 HUMAN PRESCRIPTION DRUG CARISOPRODOL CARISOPRODOL TABLET ORAL 20140731 N/A ANDA ANDA203374 Vensun Pharmaceuticals, Inc. CARISOPRODOL 350 mg/1 1000 TABLET in 1 BOTTLE (42543-700-10)
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