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
METHYLDOPATE HYDROCHLORIDE	070691	001	ANDA	METHYLDOPATE HYDROCHLORIDE	INJECTABLE;INJECTION	50MG/ML	No	No	--	1987/06/19	HOSPIRA	Discontinued
METHYLDOPA	070749	001	ANDA	METHYLDOPA	TABLET;ORAL	125MG	No	No	--	1986/02/07	PUREPAC PHARM	Discontinued
METHYLDOPA	070750	001	ANDA	METHYLDOPA	TABLET;ORAL	250MG	No	No	--	1986/02/07	PUREPAC PHARM	Discontinued
METHYLDOPA AND CHLOROTHIAZIDE	070783	001	ANDA	CHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	150MG;250MG	No	No	--	1987/11/06	PAR PHARM	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	070829	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	15MG;250MG	No	No	--	1987/03/09	SANDOZ	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	070830	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	25MG;250MG	No	No	--	1987/03/09	SANDOZ	Discontinued
METHYLDOPATE HYDROCHLORIDE	070841	001	ANDA	METHYLDOPATE HYDROCHLORIDE	INJECTABLE;INJECTION	50MG/ML	No	No	--	1987/01/02	SMITH AND NEPHEW	Discontinued
METHYLDOPATE HYDROCHLORIDE	070849	001	ANDA	METHYLDOPATE HYDROCHLORIDE	INJECTABLE;INJECTION	50MG/ML	No	No	--	1987/06/19	HOSPIRA	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	070853	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	15MG;250MG	No	No	--	1986/10/08	PUREPAC PHARM	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	070854	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	30MG;500MG	No	No	--	1986/10/08	PUREPAC PHARM	Discontinued
METHYLDOPATE HCL	071024	001	ANDA	METHYLDOPATE HYDROCHLORIDE	Injectable; Injection	50MG/ML	No	No	--	--	QUAD PHARMS	Discontinued
METHYLDOPA	071067	001	ANDA	METHYLDOPA	TABLET;ORAL	500MG	No	No	--	1986/12/05	TEVA	Discontinued
METHYLDOPA	071105	001	ANDA	METHYLDOPA	TABLET;ORAL	125MG	No	No	--	1986/12/05	TEVA	Discontinued
METHYLDOPA	071106	001	ANDA	METHYLDOPA	TABLET;ORAL	250MG	No	No	--	1986/12/05	TEVA	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	071458	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	15MG;250MG	No	No	--	1988/03/08	IVAX SUB TEVA PHARMS	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	071459	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	25MG;250MG	No	No	--	1988/03/08	IVAX SUB TEVA PHARMS	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	071460	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	30MG;500MG	No	No	--	1988/03/08	IVAX SUB TEVA PHARMS	Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE	071461	001	ANDA	HYDROCHLOROTHIAZIDE; METHYLDOPA	TABLET;ORAL	50MG;500MG	No	No	--	1988/03/08	IVAX SUB TEVA PHARMS	Discontinued
METHYLDOPA	071751	001	ANDA	METHYLDOPA	TABLET;ORAL	125MG	No	No	--	1988/03/28	HALSEY	Discontinued
METHYLDOPA	071752	001	ANDA	METHYLDOPA	TABLET;ORAL	250MG	No	No	--	1988/03/28	HALSEY	Discontinued