产品NDC49999-060
产品类型HUMAN PRESCRIPTION DRUG
商品名ACETAMINOPHEN AND CODEINE PHOSPHATE
商品名后缀
通用名ACETAMINOPHEN AND CODEINE PHOSPHATE
剂型TABLET
给药途径ORAL
上市日期20110914
中止上市日期
市场分类ANDA
申请号ANDA040419
标签持有者Lake Erie Medical DBA Quality Care Products LLC
活性成分ACETAMINOPHEN; CODEINE PHOSPHATE
规格300; 30
规格单位mg/1; mg/1
药学分类Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEACIII N 20201231
药品包装规格及说明书信息
产品NDC NDC包装代码 包装描述 药品说明书
49999-06049999-060-00100 TABLET in 1 BOTTLE (49999-060-00) 20110914 N N药品说明书及标签信息
49999-06049999-060-01120 TABLET in 1 BOTTLE (49999-060-01) 20110914 N N药品说明书及标签信息
49999-06049999-060-2020 TABLET in 1 BOTTLE (49999-060-20) 20110914 N N药品说明书及标签信息
49999-06049999-060-2424 TABLET in 1 BOTTLE (49999-060-24) 20110914 N N药品说明书及标签信息
49999-06049999-060-3030 TABLET in 1 BOTTLE (49999-060-30) 20110914 N N药品说明书及标签信息
49999-06049999-060-5050 TABLET in 1 BOTTLE (49999-060-50) 20110914 N N药品说明书及标签信息
49999-06049999-060-6060 TABLET in 1 BOTTLE (49999-060-60) 20110914 N N药品说明书及标签信息
49999-06049999-060-9090 TABLET in 1 BOTTLE (49999-060-90) 20110914 N N药品说明书及标签信息