Immucox 5 Formulation:   Each dose contains:   Eimeria acervulina (502-13, Ceva Strain) ..........>151oocysts Eimaria brunetti (505-13, Ceva Strain) .........>40 oocysts Eimeria maxima (503-13, Guelph Strain) ........>50 oocysts Eimeria necatrix (506-13, Ceva Strain) ..............51 oocysts Eimeria tenella (504-13, Ceva Strain).............25 oocysts Suspension (Oral) Philippines - English - FDA (Food And Drug Administration)

immucox 5 formulation: each dose contains: eimeria acervulina (502-13, ceva strain) ..........>151oocysts eimaria brunetti (505-13, ceva strain) .........>40 oocysts eimeria maxima (503-13, guelph strain) ........>50 oocysts eimeria necatrix (506-13, ceva strain) ..............51 oocysts eimeria tenella (504-13, ceva strain).............25 oocysts suspension (oral)

ceva animal health (philippines), inc. - live eimeria acervulina , eimeria brunetti , eimeria maxima , eimeria necatrix , eimeria tenella oocyst vaccine (vet.) - suspension (oral) - formulation: each dose contains: eimeria acervulina (502-13, ceva strain) ..........>151oocysts eimaria brunetti (505-13, ceva strain) .........>40 oocysts eimeria maxima (503-13, guelph strain) ........>50 oocysts eimeria necatrix (506-13, ceva strain) ..............51 oocysts eimeria tenella (504-13, ceva strain).............25 oocysts

Tarceva European Union - English - EMA (European Medicines Agency)

tarceva

roche registration gmbh - erlotinib - carcinoma, non-small-cell lung; pancreatic neoplasms - antineoplastic agents - non-small cell lung cancer (nsclc)tarceva is also indicated for switch maintenance treatment in patients with locally advanced or metastatic non-small cell lung cancer with egfr activating mutations and stable disease after first-line chemotherapy.tarceva is also indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen.in patients with tumours without egfr activating mutations, tarceva is indicated when other treatment options are not considered suitable.when prescribing tarceva, factors associated with prolonged survival should be taken into account.no survival benefit or other clinically relevant effects of the treatment have been demonstrated in patients with epidermal growth factor receptor (egfr)-ihc - negative tumours.pancreatic cancertarceva in combination with gemcitabine is indicated for the treatment of patients with metastatic pancreatic cancer.when prescribing tarceva, factors associated with prolonged survival should be taken into account.

TARCEVA erlotinib 150 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

tarceva erlotinib 150 mg tablet blister pack

roche products pty ltd - erlotinib hydrochloride, quantity: 163.93 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; sodium starch glycollate; magnesium stearate; sodium lauryl sulfate; lactose monohydrate; titanium dioxide; hypromellose; hyprolose; macrogol 400 - non-small cell lung cancer: tarceva is indicated for the first-line treatment of patients with advanced (stage iiib) or metastatic (stage iv) non-small cell lung cancer (nsclc) with activating egfr mutations. tarceva is indicated for maintenance therapy in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating egfr mutations who have not progressed on first-line chemotherapy. tarceva is also indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of prior chemotherapy. pancreatic cancer: tarceva in combination with gemcitabine is indicated for the treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.

TARCEVA erlotinib 100 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

tarceva erlotinib 100 mg tablet blister pack

roche products pty ltd - erlotinib hydrochloride, quantity: 109.29 mg - tablet, film coated - excipient ingredients: sodium lauryl sulfate; sodium starch glycollate; microcrystalline cellulose; magnesium stearate; lactose monohydrate; titanium dioxide; hypromellose; hyprolose; macrogol 400 - non-small cell lung cancer: tarceva is indicated for the first-line treatment of patients with advanced (stage iiib) or metastatic (stage iv) non-small cell lung cancer (nsclc) with activating egfr mutations. tarceva is indicated for maintenance therapy in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating egfr mutations who have not progressed on first-line chemotherapy. tarceva is also indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of prior chemotherapy. pancreatic cancer: tarceva in combination with gemcitabine is indicated for the treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.

TARCEVA erlotinib 25 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

tarceva erlotinib 25 mg tablet blister pack

roche products pty ltd - erlotinib hydrochloride, quantity: 27.32 mg - tablet, film coated - excipient ingredients: magnesium stearate; microcrystalline cellulose; lactose monohydrate; sodium lauryl sulfate; sodium starch glycollate; titanium dioxide; hypromellose; hyprolose; macrogol 400 - non-small cell lung cancer: tarceva is indicated for the first-line treatment of patients with advanced (stage iiib) or metastatic (stage iv) non-small cell lung cancer (nsclc) with activating egfr mutations. tarceva is indicated for maintenance therapy in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating egfr mutations who have not progressed on first-line chemotherapy. tarceva is also indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of prior chemotherapy. pancreatic cancer: tarceva in combination with gemcitabine is indicated for the treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.

Spironolactone Ceva European Union - English - EMA (European Medicines Agency)

spironolactone ceva

ceva santé animale - spironolactone - diuretics - dogs - for use in combination with standard therapy (including diuretic support, where necessary) for the treatment of congestive heart failure caused by valvular regurgitation in dogs.

CEVA KETAMINE INJECTION Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

ceva ketamine injection

ceva animal health pty ltd - ketamine as ketamine hydrochloride - parenteral liquid/solution/suspension - ketamine as ketamine hydrochloride anaesthetic active 100.0 mg/ml - anaesthetics/analgesics - birds | camel | cat | cattle | deer | dog | goat | horse | kangaroo | koala | pigs | reptile | sheep | wombat | aviary bird | be - dissociative anaesthetic

TARCEVA 100 MG Israel - English - Ministry of Health

tarceva 100 mg

roche pharmaceuticals (israel) ltd - erlotinib - film coated tablets - erlotinib 100 mg - erlotinib - non-small cell lung cancer (nsclc):tarceva is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations.tarceva is indicated for switch maintenance treatment in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations and stable disease after first-line chemotherapy.tarceva is indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen.pancreatic cancer:tarceva is indicated in combination with gemcitabine for the first-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.

TARCEVA 100 MG Israel - English - Ministry of Health

tarceva 100 mg

roche pharmaceuticals (israel) ltd - erlotinib - film coated tablets - erlotinib 100 mg - erlotinib - non-small cell lung cancer (nsclc):tarceva is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations.tarceva is indicated for switch maintenance treatment in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations and stable disease after first-line chemotherapy.tarceva is indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen.pancreatic cancer:tarceva is indicated in combination with gemcitabine for the first-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.

TARCEVA 150 MG Israel - English - Ministry of Health

tarceva 150 mg

roche pharmaceuticals (israel) ltd - erlotinib - film coated tablets - erlotinib 150 mg - erlotinib - non-small cell lung cancer (nsclc):tarceva is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations.tarceva is indicated for switch maintenance treatment in patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with egfr activating mutations and stable disease after first-line chemotherapy.tarceva is indicated for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen.pancreatic cancer:tarceva is indicated in combination with gemcitabine for the first-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer.