New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - tenecteplase 30mg (recombinant) - powder for injection - 30 mg - active: tenecteplase 30mg (recombinant) excipient: arginine phosphoric acid polysorbate 20 water for injection - metalyse is indicated for the thrombolytic treatment of the acute phase of myocardial infarction (ami). treatment should be initiated as soon as possible after symptom onset. treatment can be initiated within 12 hours of symptom onset.

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - tenecteplase 40mg (recombinant) - powder for injection - 40 mg - active: tenecteplase 40mg (recombinant) excipient: arginine phosphoric acid polysorbate 20 water for injection - metalyse is indicated for the thrombolytic treatment of the acute phase of myocardial infarction (ami). treatment should be initiated as soon as possible after symptom onset. treatment can be initiated within 12 hours of symptom onset.

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - tenecteplase 50mg (recombinant) - powder for injection - 50 mg - active: tenecteplase 50mg (recombinant) excipient: arginine phosphoric acid polysorbate 20 water for injection - metalyse is indicated for the thrombolytic treatment of the acute phase of myocardial infarction (ami). treatment should be initiated as soon as possible after symptom onset. treatment can be initiated within 12 hours of symptom onset.

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - 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

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - 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.

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - meloxicam 7.5mg - capsule - 7.5 mg - active: meloxicam 7.5mg excipient: lactose monohydrate magnesium stearate maize starch sodium citrate dihydrate

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - dipyridamole 25mg - tablet - 25 mg - active: dipyridamole 25mg excipient: magnesium stearate - indicated as an adjunct to oral anticoagulation for the prophylaxis of thromboembolism associated with mechanical prosthetic heart valves.

New Zealand - engelsk - Medsafe (Medicines Safety Authority)

boehringer ingelheim (nz) ltd - dipyridamole 150mg;   - modified release capsule - 150 mg - active: dipyridamole 150mg   excipient: acacia acetone dimeticone ethanol gelatin hypromellose hypromellose phthalate isopropyl alcohol methacrylic acid copolymer povidone purified talc purified water stearic acid tartaric acid triacetin

Serbia - serbisk - Агенција за лекове и медицинска средства Србије (Agencija za lekove i medicins)

boehringer ingelheim serbia d.o.o. beograd - афатиниб - film tableta - 20mg

Serbia - serbisk - Агенција за лекове и медицинска средства Србије (Agencija za lekove i medicins)

boehringer ingelheim serbia d.o.o. beograd - афатиниб - film tableta - 30mg