美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=METHOTREXATE SODIUM"
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
METHOTREXATE SODIUM 088935 001 ANDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 20MG BASE/VIAL No No -- 1985/10/11 ABRAXIS PHARM Discontinued
METHOTREXATE SODIUM 088936 001 ANDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 50MG BASE/VIAL No No -- 1985/10/11 ABRAXIS PHARM Discontinued
METHOTREXATE SODIUM 088937 001 ANDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 100MG BASE/VIAL No No -- 1985/10/11 ABRAXIS PHARM Discontinued
METHOTREXATE SODIUM 089293 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 20MG BASE/VIAL No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 089294 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 50MG BASE/VIAL No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 089295 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 100MG BASE/VIAL No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 089296 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 250MG BASE/VIAL No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 089308 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 25MG BASE/ML No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 089309 001 ANDA METHOTREXATE SODIUM Injectable; Injection EQ 25MG BASE/ML No No -- -- QUAD PHARMS Discontinued
METHOTREXATE SODIUM 008085 002 NDA METHOTREXATE SODIUM TABLET;ORAL EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1953/12/07 Approved Prior to Jan 1, 1982 STRIDES PHARMA Discontinued
METHOTREXATE SODIUM 011719 001 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 20MG BASE/VIAL Yes No 1959/08/10 Approved Prior to Jan 1, 1982 HOSPIRA Discontinued
METHOTREXATE SODIUM 011719 003 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 50MG BASE/VIAL Yes No 1959/08/10 Approved Prior to Jan 1, 1982 HOSPIRA Discontinued
METHOTREXATE SODIUM 011719 004 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 2.5MG BASE/ML Yes No 1959/08/10 Approved Prior to Jan 1, 1982 HOSPIRA Discontinued
METHOTREXATE SODIUM 011719 005 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 25MG BASE/ML Yes No 1959/08/10 Approved Prior to Jan 1, 1982 HOSPIRA Discontinued
METHOTREXATE SODIUM 011719 006 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 100MG BASE/VIAL Yes No 1959/08/10 Approved Prior to Jan 1, 1982 HOSPIRA Discontinued
METHOTREXATE SODIUM PRESERVATIVE FREE 011719 009 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL Yes No 1959/08/10 1988/04/07 HOSPIRA Discontinued
METHOTREXATE SODIUM 011719 010 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 50MG BASE/2ML (EQ 25MG BASE/ML) Yes Yes 1959/08/10 2004/12/15 HOSPIRA Prescription
METHOTREXATE SODIUM PRESERVATIVE FREE 011719 012 NDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 1GM BASE/40ML (EQ 25MG BASE/ML) Yes Yes 1959/08/10 2005/04/13 HOSPIRA Prescription
METHOTREXATE SODIUM 088648 001 ANDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 25MG BASE/ML No No 1986/05/09 1986/05/09 NORBROOK Discontinued
METHOTREXATE SODIUM 089263 001 ANDA METHOTREXATE SODIUM INJECTABLE;INJECTION EQ 25MG BASE/ML No No 1986/06/13 1986/06/13 ABRAXIS PHARM Discontinued
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