美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=METHYLDOPA"
符合检索条件的记录共 104 条
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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
METHYLDOPA 070192 001 ANDA METHYLDOPA TABLET;ORAL 125MG No No -- 1986/04/25 ROXANE Discontinued
METHYLDOPA 070193 001 ANDA METHYLDOPA TABLET;ORAL 250MG No No -- 1986/04/25 ROXANE Discontinued
METHYLDOPA 070194 001 ANDA METHYLDOPA TABLET;ORAL 500MG No No -- 1986/04/25 ROXANE Discontinued
METHYLDOPA 070245 001 ANDA METHYLDOPA TABLET;ORAL 125MG No No -- 1986/02/25 WATSON LABS Discontinued
METHYLDOPA 070246 001 ANDA METHYLDOPA TABLET;ORAL 250MG No No -- 1986/02/25 WATSON LABS Discontinued
METHYLDOPA 070247 001 ANDA METHYLDOPA TABLET;ORAL 500MG No No -- 1986/02/25 WATSON LABS Discontinued
METHYLDOPA 070260 001 ANDA METHYLDOPA TABLET;ORAL 125MG No No -- 1985/06/24 WATSON LABS Discontinued
METHYLDOPA 070261 001 ANDA METHYLDOPA TABLET;ORAL 250MG No No -- 1985/06/24 WATSON LABS Discontinued
METHYLDOPA 070262 001 ANDA METHYLDOPA TABLET;ORAL 500MG No No -- 1985/06/24 WATSON LABS Discontinued
METHYLDOPA 070331 001 ANDA METHYLDOPA TABLET;ORAL 125MG No No -- 1986/04/15 PARKE DAVIS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070365 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 15MG;250MG No No -- 1986/03/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070366 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1986/04/16 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070367 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 30MG;500MG No No -- 1986/03/19 WATSON LABS Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070368 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1986/04/16 WATSON LABS Discontinued
METHYLDOPA 070452 001 ANDA METHYLDOPA TABLET;ORAL 500MG No No -- 1986/02/07 PUREPAC PHARM Discontinued
METHYLDOPA AND CHLOROTHIAZIDE 070654 001 ANDA CHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 250MG;250MG No No -- 1987/11/06 PAR PHARM Discontinued
METHYLDOPA 070669 001 ANDA METHYLDOPA TABLET;ORAL 250MG No No -- 1989/06/23 SUPERPHARM Discontinued
METHYLDOPA 070670 001 ANDA METHYLDOPA TABLET;ORAL 500MG No No -- 1989/06/23 SUPERPHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070688 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 25MG;250MG No No -- 1986/04/24 PUREPAC PHARM Discontinued
METHYLDOPA AND HYDROCHLOROTHIAZIDE 070689 001 ANDA HYDROCHLOROTHIAZIDE; METHYLDOPA TABLET;ORAL 50MG;500MG No No -- 1986/04/24 PUREPAC PHARM Discontinued
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