美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=REDITREX"
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) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 001 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 7.5MG/0.3ML (7.5MG/0.3ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 002 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 10MG/0.4ML (10MG/0.4ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 002 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 10MG/0.4ML (10MG/0.4ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 003 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 12.5MG/0.5ML (12.5MG/0.5ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 003 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 12.5MG/0.5ML (12.5MG/0.5ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 004 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 15MG/0.6ML (15MG/0.6ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 004 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 15MG/0.6ML (15MG/0.6ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 005 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 17.5MG/0.7ML (17.5MG/0.7ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 005 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 17.5MG/0.7ML (17.5MG/0.7ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 006 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 20MG/0.8ML (20MG/0.8ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 006 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 20MG/0.8ML (20MG/0.8ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 007 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 22.5MG/ML (22.5MG/ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 007 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 22.5MG/ML (22.5MG/ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 008 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 25MG/1ML (25MG/1ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
REDITREX 210737 008 NDA METHOTREXATE SOLUTION;SUBCUTANEOUS 25MG/1ML (25MG/1ML) No No 2019/11/27 2019/11/27 CUMBERLAND PHARMS Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2020 DrugFuture->U.S. FDA Drugs Database