PROTECH C3 + 2I Austràlia - anglès - APVMA (Australian Pesticides and Veterinary Medicines Authority)

protech c3 + 2i

boehringer ingelheim animal health australia pty. ltd. - leptospirosis - dog - leptospira icterohaemorrhagiae; canine adeno virus type 2; canine coronavirus vaccine - antigen; canine distemper virus strain onderstepoort; canine parvo virus - misc. vaccines or anti sera - leptospirosis - dog - leptospira icterohaemorrhagiae vaccine active 0.0 u; canine adeno virus type 2 vaccine-viral active 0.0 u; canine coronavirus vaccine - antigen vaccine-viral active 0.0 u; canine distemper virus strain onderstepoort vaccine-viral active 0.0 u; canine parvo virus vaccine-viral active 0.0 u - immunotherapy - dog - over 6 weeks old - canine adenovirus - type 1 | canine adenovirus - type 2 | canine coronavirus | canine distemper | canine parvovirus | leptospira icterohaemorrhagiae | parvovirus

PROTECH C4 + 2I Austràlia - anglès - APVMA (Australian Pesticides and Veterinary Medicines Authority)

protech c4 + 2i

boehringer ingelheim animal health australia pty. ltd. - canine parainfluenza; leptospira icterohaemorrhagiae antigen; canine adeno virus type 2; canine coronavirus vaccine - antigen; canine distemper virus; canine parvo virus - misc. vaccines or anti sera - canine parainfluenza vaccine active 0.0 undefined; leptospira icterohaemorrhagiae antigen vaccine-antigen active 0.0 undefined; canine adeno virus type 2 vaccine-viral active 0.0 undefined; canine coronavirus vaccine - antigen vaccine-viral active 0.0 undefined; canine distemper virus vaccine-viral active 0.0 undefined; canine parvo virus vaccine-viral active 0.0 undefined - immunotherapy - dog - over 6 weeks old - canine adenovirus - type 1 | canine adenovirus - type 2 | canine coronavirus | canine distemper | canine parainfluenza | canine parvovirus | leptospira icterohaemorrhagiae | parvovirus

Actilyse Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

actilyse

boehringer ingelheim (nz) limited - alteplase 10mg - injection with diluent - 10 mg - active: alteplase 10mg excipient: arginine nitrogen phosphoric acid polysorbate 80 water for injection - actilyse is indicated for fibrinolytic therapy in acute thrombotic artery occlusion to restore coronary artery patency, reduce infarct size, preserve ventricular function, prevent cardiac insufficiency and reduce mortality · 90 minutes (accelerated) dose regimen: for patients in whom treatment can be started within 6 h of symptom onset; · 3 hour dose regimen: for patients in whom treatment can be started between 6 - 12 hrs after symptom onset.

Actilyse Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

actilyse

boehringer ingelheim (nz) limited - alteplase 20mg - injection with diluent - 20 mg - active: alteplase 20mg excipient: arginine nitrogen phosphoric acid polysorbate 80 water for injection - actilyse is indicated for fibrinolytic therapy in acute thrombotic artery occlusion to restore coronary artery patency, reduce infarct size, preserve ventricular function, prevent cardiac insufficiency and reduce mortality · 90 minutes (accelerated) dose regimen: for patients in whom treatment can be started within 6 h of symptom onset; · 3 hour dose regimen: for patients in whom treatment can be started between 6 - 12 hrs after symptom onset.

Actilyse Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

actilyse

boehringer ingelheim (nz) limited - alteplase 50mg - injection with diluent - 50 mg - active: alteplase 50mg excipient: arginine nitrogen phosphoric acid polysorbate 80 water for injection - actilyse is indicated for fibrinolytic therapy in acute thrombotic artery occlusion to restore coronary artery patency, reduce infarct size, preserve ventricular function, prevent cardiac insufficiency and reduce mortality · 90 minutes (accelerated) dose regimen: for patients in whom treatment can be started within 6 h of symptom onset; · 3 hour dose regimen: for patients in whom treatment can be started between 6 - 12 hrs after symptom onset.

Atrovent Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

atrovent

boehringer ingelheim (nz) limited - ipratropium bromide monohydrate 0.021mg equivalent to 0.020 mg/dose ipratropium bromide anhydrous - aerosol inhaler, metered dose - 20 mcg/dose - active: ipratropium bromide monohydrate 0.021mg equivalent to 0.020 mg/dose ipratropium bromide anhydrous excipient: citric acid ethanol nitrogen norflurane purified water - atrovent is indicated as a bronchodilator for maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease, including chronic bronchitis, emphysema and asthma.

Dixarit Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

dixarit

boehringer ingelheim (nz) limited - clonidine hydrochloride 25ug - tablet - 25 mcg - active: clonidine hydrochloride 25ug excipient: acacia amylodextrin calcium hydrogen phosphate dihydrate carnauba wax colloidal silicon dioxide indigo carmine   lactose monohydrate macrogol 6000 magnesium stearate maize starch methyl hydroxybenzoate povidone   propyl hydroxybenzoate purified talc sucrose titanium dioxide white beeswax

Imukin Nova Zelanda - anglès - Medsafe (Medicines Safety Authority)

imukin

boehringer ingelheim (nz) limited - interferon gamma-1b 200 µg/ml - solution for injection - 3 miu/0.5ml - active: interferon gamma-1b 200 µg/ml excipient: mannitol polysorbate 20 sodium succinate succinic acid water for injection - imukin is indicated as an adjunct for reduction of the frequency of serious infections in patients with chronic granulomatous disease (cgd). the benefits of imukin have been most marked in children with cgd although imukin may be used in adult patients.