Lenalidomide Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

lenalidomide te arai

te arai biofarma limited - lenalidomide 7.5mg - capsule - 7.5 mg - active: lenalidomide 7.5mg excipient: brilliant blue fcf croscarmellose sodium erythrosine gelatin lactose magnesium stearate microcrystalline cellulose sunset yellow fcf titanium dioxide - lenalidomide te arai is indicated for treatment of patients with transfusion-dependent anaemia due to low- or intermediate-1 risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.

Equilis Prequenza Te यूरोपीय संघ - अंग्रेज़ी - EMA (European Medicines Agency)

equilis prequenza te

intervet international bv - equine influenza-virus strains: a/equine-2/south africa/4/03, a/equine-2/newmarket/2/93, tetanus toxoid - equine influenza virus + clostridium - horses - active immunisation of horses from six months of age against equine influenza to reduce clinical signs and virus excretion after infection, and active immunisation against tetanus to prevent mortality.

Cinacalcet Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

cinacalcet te arai

te arai biofarma limited - cinacalcet hydrochloride 33.075mg equivalent to 30 mg cinacalcet - film coated tablet - 30 mg - active: cinacalcet hydrochloride 33.075mg equivalent to 30 mg cinacalcet excipient: colloidal silicon dioxide magnesium stearate microcrystalline cellulose opadry green 85f21867 povidone sodium starch glycolate starch - latest regulatory activity

Cinacalcet Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

cinacalcet te arai

te arai biofarma limited - cinacalcet hydrochloride 66.15mg equivalent to 60 mg cinacalcet - film coated tablet - 60 mg - active: cinacalcet hydrochloride 66.15mg equivalent to 60 mg cinacalcet excipient: colloidal silicon dioxide magnesium stearate microcrystalline cellulose opadry green 85f21867 povidone sodium starch glycolate starch - latest regulatory activity

Cinacalcet Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

cinacalcet te arai

te arai biofarma limited - cinacalcet hydrochloride 99.225mg equivalent to 90 mg cinacalcet - film coated tablet - 90 mg - active: cinacalcet hydrochloride 99.225mg equivalent to 90 mg cinacalcet excipient: colloidal silicon dioxide magnesium stearate microcrystalline cellulose opadry green 85f21867 povidone sodium starch glycolate starch - latest regulatory activity

Lenalidomide Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

lenalidomide te arai

te arai biofarma limited - lenalidomide 10mg - capsule - 10 mg - active: lenalidomide 10mg excipient: allura red ac brilliant blue fcf croscarmellose sodium gelatin lactose magnesium stearate microcrystalline cellulose sunset yellow fcf tartrazine titanium dioxide - lenalidomide te arai is indicated for treatment of patients with transfusion-dependent anaemia due to low- or intermediate-1 risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.

Lenalidomide Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

lenalidomide te arai

te arai biofarma limited - lenalidomide 15mg - capsule - 15 mg - active: lenalidomide 15mg excipient: allura red ac brilliant blue fcf croscarmellose sodium gelatin iron oxide black iron oxide red iron oxide yellow lactose magnesium stearate microcrystalline cellulose tartrazine titanium dioxide - lenalidomide te arai is indicated for treatment of patients with transfusion-dependent anaemia due to low- or intermediate-1 risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.

Lenalidomide Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

lenalidomide te arai

te arai biofarma limited - lenalidomide 25mg - capsule - 25 mg - active: lenalidomide 25mg excipient: croscarmellose sodium gelatin black sw-9007 printing ink lactose magnesium stearate microcrystalline cellulose titanium dioxide water - lenalidomide te arai is indicated for treatment of patients with transfusion-dependent anaemia due to low- or intermediate-1 risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.

Lenalidomide Te Arai न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

lenalidomide te arai

te arai biofarma limited - lenalidomide 5mg - capsule - 5 mg - active: lenalidomide 5mg excipient: brilliant blue fcf croscarmellose sodium gelatin iron oxide black iron oxide red iron oxide yellow lactose magnesium stearate microcrystalline cellulose sunset yellow fcf titanium dioxide - lenalidomide te arai is indicated for treatment of patients with transfusion-dependent anaemia due to low- or intermediate-1 risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.

TE-DASATINIB dasatinib 50 mg film-coated tablet bottle ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

te-dasatinib dasatinib 50 mg film-coated tablet bottle

teva pharma australia pty ltd - dasatinib, quantity: 50 mg - tablet, film coated - excipient ingredients: magnesium stearate; microcrystalline cellulose; croscarmellose sodium; lactose monohydrate; hyprolose; titanium dioxide; hypromellose; triacetin - dasatinib is indicated for the treatment of adults aged 18 years or over with: ? newly diagnosed philadelphia chromosome positive (ph+) chronic myeloid leukaemia in the chronic phase. ? chronic, accelerated or myeloid or lymphoid blast phase chronic myeloid leukaemia with resistance or intolerance to prior therapy including imatinib. ? newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia integrated with chemotherapy. ? philadelphia chromosome positive acute lymphoblastic leukaemia with resistance or intolerance to prior therapy.,dasatinib is indicated for the treatment of paediatric patients with: ? ph+ cml in the chronic phase. ? newly diagnosed ph+ all in combination with chemotherapy.