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=ANDA075993"
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
0527-5125-78 0527-5125 HUMAN PRESCRIPTION DRUG LACTULOSE LACTULOSE SOLUTION ORAL 20010726 N/A ANDA ANDA075993 Lannett Company, Inc. LACTULOSE 10 g/15mL 946 mL in 1 BOTTLE (0527-5125-78)
0527-5125-82 0527-5125 HUMAN PRESCRIPTION DRUG LACTULOSE LACTULOSE SOLUTION ORAL 20010726 N/A ANDA ANDA075993 Lannett Company, Inc. LACTULOSE 10 g/15mL 1892 mL in 1 BOTTLE (0527-5125-82)
0527-5125-70 0527-5125 HUMAN PRESCRIPTION DRUG LACTULOSE LACTULOSE SOLUTION ORAL 20010726 N/A ANDA ANDA075993 Lannett Company, Inc. LACTULOSE 10 g/15mL 473 mL in 1 BOTTLE (0527-5125-70)
0527-5125-68 0527-5125 HUMAN PRESCRIPTION DRUG LACTULOSE LACTULOSE SOLUTION ORAL 20010726 N/A ANDA ANDA075993 Lannett Company, Inc. LACTULOSE 10 g/15mL 237 mL in 1 BOTTLE (0527-5125-68)
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