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=ANDA217914"
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
0121-1930-30 0121-1930 HUMAN PRESCRIPTION DRUG Lactulose Lactulose POWDER, FOR SOLUTION ORAL 20250317 N/A ANDA ANDA217914 PAI Holdings, LLC dba PAI Pharma LACTULOSE 20 g/20g 30 POUCH in 1 CARTON (0121-1930-30) / 20 g in 1 POUCH (0121-1930-01)
0121-0965-30 0121-0965 HUMAN PRESCRIPTION DRUG Lactulose Lactulose POWDER, FOR SOLUTION ORAL 20250317 N/A ANDA ANDA217914 PAI Holdings, LLC dba PAI Pharma LACTULOSE 10 g/10g 30 POUCH in 1 CARTON (0121-0965-30) / 10 g in 1 POUCH (0121-0965-01)
73352-900-15 73352-900 HUMAN PRESCRIPTION DRUG Lactulose Lactulose POWDER, FOR SOLUTION ORAL 20250913 N/A ANDA ANDA217914 Trifluent Pharma, Inc. LACTULOSE 10 g/10g 15 POUCH in 1 CARTON (73352-900-15) / 10 g in 1 POUCH (73352-900-01)
73352-905-15 73352-905 HUMAN PRESCRIPTION DRUG Lactulose Lactulose POWDER, FOR SOLUTION ORAL 20250913 N/A ANDA ANDA217914 Trifluent Pharma, Inc. LACTULOSE 20 g/20g 15 POUCH in 1 CARTON (73352-905-15) / 20 g in 1 POUCH (73352-905-01)
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