美国FDA药品数据库-药物在线

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