美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=COMPAZINE"
符合检索条件的记录共 15 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
COMPAZINE 011276 001 NDA PROCHLORPERAZINE EDISYLATE CONCENTRATE;ORAL EQ 10MG BASE/ML Yes No -- Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 010571 001 NDA PROCHLORPERAZINE MALEATE TABLET;ORAL EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1956/10/23 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 010571 002 NDA PROCHLORPERAZINE MALEATE TABLET;ORAL EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1956/10/23 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 010571 003 NDA PROCHLORPERAZINE MALEATE TABLET;ORAL EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1956/10/23 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 010742 002 NDA PROCHLORPERAZINE EDISYLATE INJECTABLE;INJECTION EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1957/04/08 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011000 001 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 10MG BASE No No 1957/06/05 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011000 002 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 15MG BASE No No 1957/06/05 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011000 003 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 30MG BASE No No 1957/06/05 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011000 004 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE No No 1957/06/05 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011188 001 NDA PROCHLORPERAZINE EDISYLATE SYRUP;ORAL EQ 5MG BASE/5ML No No 1957/12/10 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011127 001 NDA PROCHLORPERAZINE SUPPOSITORY;RECTAL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1959/01/26 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011127 002 NDA PROCHLORPERAZINE SUPPOSITORY;RECTAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1959/01/26 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 011127 003 NDA PROCHLORPERAZINE SUPPOSITORY;RECTAL 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1959/01/26 Approved Prior to Jan 1, 1982 GLAXOSMITHKLINE Discontinued
COMPAZINE 021019 001 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 10MG BASE No No 1999/10/06 1999/10/06 GLAXOSMITHKLINE Discontinued
COMPAZINE 021019 002 NDA PROCHLORPERAZINE MALEATE CAPSULE, EXTENDED RELEASE;ORAL EQ 15MG BASE No No 1999/10/06 1999/10/06 GLAXOSMITHKLINE Discontinued
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