产品NDC0406-0484
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20010531
中止上市日期
市场分类ANDA
申请号ANDA040419
标签持有者SpecGx 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 20211231
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
0406-04840406-0484-01100 TABLET in 1 BOTTLE (0406-0484-01) 20010531 N N药品说明书及标签信息
0406-04840406-0484-0330 TABLET in 1 BOTTLE (0406-0484-03) 20010531 N N药品说明书及标签信息
0406-04840406-0484-101000 TABLET in 1 BOTTLE (0406-0484-10) 20010531 N N药品说明书及标签信息
0406-04840406-0484-2020 TABLET in 1 BOTTLE (0406-0484-20) 20010531 N N药品说明书及标签信息
0406-04840406-0484-231 TABLET in 1 BLISTER PACK (0406-0484-23) 20010531 N N药品说明书及标签信息
0406-04840406-0484-5050 TABLET in 1 BOTTLE (0406-0484-50) 20010531 N N药品说明书及标签信息
0406-04840406-0484-62100 TABLET in 1 BLISTER PACK (0406-0484-62) 20010531 N N药品说明书及标签信息