美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 040109 001 ANDA ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE CAPSULE;ORAL 356.4MG;30MG;16MG No No 1997/08/26 1997/08/26 MIKART Discontinued
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 040316 001 ANDA ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE TABLET;ORAL 712.8MG;60MG;32MG No No 1999/04/28 1999/04/28 MIKART Discontinued
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 040637 001 ANDA ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE TABLET;ORAL 712.8MG;60MG;32MG No No 2006/09/22 2006/09/22 WEST-WARD PHARM CORP Discontinued
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 040688 001 ANDA ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE CAPSULE;ORAL 356.4MG;30MG;16MG No No 2007/04/03 2007/04/03 WRASER PHARMS LLC Discontinued
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 040701 001 ANDA ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE TABLET;ORAL 712.8MG;60MG;32MG No No 2007/04/03 2007/04/03 BOCA PHARMA LLC Discontinued
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