美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=HALDOL"
符合检索条件的记录共 11 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
HALDOL SOLUTAB 017079 001 NDA HALOPERIDOL TABLET;ORAL 1MG No No -- Approved Prior to Jan 1, 1982 ORTHO MCNEIL PHARM Discontinued
HALDOL 015921 001 NDA HALOPERIDOL TABLET;ORAL 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015921 002 NDA HALOPERIDOL TABLET;ORAL 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015921 003 NDA HALOPERIDOL TABLET;ORAL 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015921 004 NDA HALOPERIDOL TABLET;ORAL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015921 005 NDA HALOPERIDOL TABLET;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015921 006 NDA HALOPERIDOL TABLET;ORAL 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 1982/02/02 ORTHO MCNEIL Discontinued
HALDOL 015922 001 NDA HALOPERIDOL LACTATE CONCENTRATE;ORAL EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1967/04/12 Approved Prior to Jan 1, 1982 ORTHO MCNEIL Discontinued
HALDOL 015923 001 NDA HALOPERIDOL LACTATE INJECTABLE;INJECTION EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1971/05/18 Approved Prior to Jan 1, 1982 JANSSEN PHARMS Discontinued
HALDOL 018701 001 NDA HALOPERIDOL DECANOATE INJECTABLE;INJECTION EQ 50MG BASE/ML Yes Yes 1986/01/14 1986/01/14 JANSSEN PHARMS Prescription
HALDOL 018701 002 NDA HALOPERIDOL DECANOATE INJECTABLE;INJECTION EQ 100MG BASE/ML Yes Yes 1986/01/14 1997/01/31 JANSSEN PHARMS Prescription
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