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
MUCINEX	021282	001	NDA	GUAIFENESIN	TABLET, EXTENDED RELEASE;ORAL	600MG	Yes	No	2002/07/12	2002/07/12	RB HLTH	Over-the-counter
MUCINEX	021282	002	NDA	GUAIFENESIN	TABLET, EXTENDED RELEASE;ORAL	1.2GM	Yes	Yes	2002/07/12	2002/12/18	RB HLTH	Over-the-counter
MUCINEX DM	021620	001	NDA	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN	TABLET, EXTENDED RELEASE;ORAL	60MG;1.2GM	Yes	Yes	2004/04/29	2004/04/29	RB HLTH	Over-the-counter
MUCINEX DM	021620	002	NDA	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN	TABLET, EXTENDED RELEASE;ORAL	30MG;600MG	Yes	No	2004/04/29	2004/04/29	RB HLTH	Over-the-counter
MUCINEX D	021585	001	NDA	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	600MG;60MG	Yes	No	2004/06/22	2004/06/22	RB HLTH	Over-the-counter
MUCINEX D	021585	002	NDA	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	1.2GM;120MG	Yes	Yes	2004/06/22	2004/06/22	RB HLTH	Over-the-counter