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
TRIPROLIDINE HYDROCHLORIDE	085610	001	ANDA	TRIPROLIDINE HYDROCHLORIDE	TABLET;ORAL	2.5MG	No	No	--	Approved Prior to Jan 1, 1982	VITARINE	Discontinued
TRIPROLIDINE HYDROCHLORIDE	087514	001	ANDA	TRIPROLIDINE HYDROCHLORIDE	SYRUP;ORAL	1.25MG/5ML	No	No	--	1982/02/10	PHARM ASSOC	Discontinued
TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE	088578	001	ANDA	PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE	TABLET;ORAL	60MG;2.5MG	No	No	--	1985/02/21	SUPERPHARM	Discontinued
TRIPROLIDINE HYDROCHLORIDE	085094	001	ANDA	TRIPROLIDINE HYDROCHLORIDE	TABLET;ORAL	2.5MG	No	No	1977/02/07	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
TRIPROLIDINE HYDROCHLORIDE	085940	001	ANDA	TRIPROLIDINE HYDROCHLORIDE	SYRUP;ORAL	1.25MG/5ML	No	No	1979/07/13	Approved Prior to Jan 1, 1982	ALPHARMA US PHARMS	Discontinued
TRIPROLIDINE HYDROCHLORIDE, PSEUDOEPHEDRINE HYDROCHLORIDE AND CODEINE PHOSPHATE	088833	001	ANDA	CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE	SYRUP;ORAL	10MG/5ML;30MG/5ML;1.25MG/5ML	No	No	1984/11/16	1984/11/16	WOCKHARDT	Discontinued
TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE	085273	001	ANDA	PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE	TABLET;ORAL	60MG;2.5MG	No	No	1984/12/12	1984/12/12	IVAX SUB TEVA PHARMS	Discontinued
TRIPROLIDINE HYDROCHLORIDE	088735	001	ANDA	TRIPROLIDINE HYDROCHLORIDE	SYRUP;ORAL	1.25MG/5ML	No	No	1985/01/17	1985/01/17	HALSEY	Discontinued
PSEUDOEPHEDRINE HYDROCHLORIDE AND TRIPROLIDINE HYDROCHLORIDE	088193	001	ANDA	PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE	TABLET;ORAL	60MG;2.5MG	No	No	1994/09/16	1983/05/17	SANDOZ	Discontinued