美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=REDITREX"
符合检索条件的记录共 16 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
REDITREX 210737 001 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 7.5MG/0.3ML (7.5MG/0.3ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 001 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 7.5MG/0.3ML (7.5MG/0.3ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 002 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 10MG/0.4ML (10MG/0.4ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 002 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 10MG/0.4ML (10MG/0.4ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 003 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 12.5MG/0.5ML (12.5MG/0.5ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 003 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 12.5MG/0.5ML (12.5MG/0.5ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 004 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 15MG/0.6ML (15MG/0.6ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 004 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 15MG/0.6ML (15MG/0.6ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 005 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 17.5MG/0.7ML (17.5MG/0.7ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 005 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 17.5MG/0.7ML (17.5MG/0.7ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 006 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 20MG/0.8ML (20MG/0.8ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 006 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 20MG/0.8ML (20MG/0.8ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 007 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 22.5MG/ML (22.5MG/ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 007 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 22.5MG/ML (22.5MG/ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 008 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 25MG/1ML (25MG/1ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
REDITREX 210737 008 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 25MG/1ML (25MG/1ML) Yes No 2019/11/27 2019/11/27 NORDIC GRP Discontinued
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