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=ANDA218366"
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
80005-118-11 80005-118 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 250 mg/1 100 TABLET in 1 BOTTLE (80005-118-11)
80005-118-14 80005-118 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 250 mg/1 500 TABLET in 1 BOTTLE (80005-118-14)
80005-118-15 80005-118 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 250 mg/1 1000 TABLET in 1 BOTTLE (80005-118-15)
80005-117-11 80005-117 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 50 mg/1 100 TABLET in 1 BOTTLE (80005-117-11)
80005-117-14 80005-117 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 50 mg/1 500 TABLET in 1 BOTTLE (80005-117-14)
80005-117-15 80005-117 HUMAN PRESCRIPTION DRUG Primidone Primidone TABLET ORAL 20240501 N/A ANDA ANDA218366 Carnegie Pharmaceuticals LLC PRIMIDONE 50 mg/1 1000 TABLET in 1 BOTTLE (80005-117-15)
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