METEX XR metformin hydrochloride 1000 mg modified release tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

metex xr metformin hydrochloride 1000 mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - metformin hydrochloride, quantity: 1000 mg - tablet, modified release - excipient ingredients: hypromellose; povidone; magnesium stearate; colloidal anhydrous silica - treatment of type 2 diabetes mellitus in adults, particularly in overweight patients, when dietary management and exercise alone does not result in adequate glycaemic control. metformin modified release tablets may be used as monotherapy or in combination with other oral antidiabetic agents, or with insulin.

SEVREDOL morphine sulfate pentahydrate 20mg tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

sevredol morphine sulfate pentahydrate 20mg tablet blister pack

mundipharma pty ltd - morphine sulfate pentahydrate, quantity: 20 mg - tablet, film coated - excipient ingredients: povidone; lactose; magnesium stearate; purified talc; pregelatinised maize starch; titanium dioxide; sunset yellow fcf aluminium lake; polyvinyl alcohol; macrogol 3350; erythrosine aluminium lake - treatment of chronic severe pain of cancer.

LAMIVUDINE/ZIDOVUDINE VIATRIS 150/300  lamivudine 150 mg / zidovudine 300 mg film-coated tablet bottle Australien - engelska - Department of Health (Therapeutic Goods Administration)

lamivudine/zidovudine viatris 150/300 lamivudine 150 mg / zidovudine 300 mg film-coated tablet bottle

alphapharm pty ltd - lamivudine, quantity: 150 mg; zidovudine, quantity: 300 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; microcrystalline cellulose; propylene glycol; magnesium stearate; sodium starch glycollate type a; titanium dioxide; hypromellose - lamivudine and zidovudine combination tablet is indicated for use alone or in combination with other antiretroviral therapies in the treatment of hiv infection.

RIAMET 20 mg /120 mg artemether/lumefantrine 20 mg/120 mg dispersible tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

riamet 20 mg /120 mg artemether/lumefantrine 20 mg/120 mg dispersible tablet blister pack

novartis pharmaceuticals australia pty ltd - artemether, quantity: 20 mg; lumefantrine, quantity: 120 mg - tablet, dispersible - excipient ingredients: microcrystalline cellulose; croscarmellose sodium; crospovidone; saccharin sodium; hypromellose; magnesium stearate; polysorbate 80; colloidal anhydrous silica; flavour - riamet tablet is indicated for the treatment of acute, uncomplicated malaria due to plasmodium falciparum in adults, children and infants of 5kg and above. riamet dispersible tablet is indicated for the treatment of acute, uncomplicated malaria due to plasmodium falciparum in children and infants weighing between 5kg and less than 35kg.

APO-GLICLAZIDE MR  30mg tablets, bottle Australien - engelska - Department of Health (Therapeutic Goods Administration)

apo-gliclazide mr 30mg tablets, bottle

arrotex pharmaceuticals pty ltd - gliclazide, quantity: 30 mg - tablet, modified release - excipient ingredients: stearic acid; hypromellose; colloidal anhydrous silica - type ii diabetes in association with dietary measures when dietary measures alone are inadequate to control blood glucose. during controlled clinical trials in patients with type ii diabetes, gliclazide mr 30 mg tablets, taken as a single daily dose, was shown to be effective long term in controlling blood glucose levels, based on monitoring of hba1c.

APO-GLICLAZIDE MR  30mg tablets, blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

apo-gliclazide mr 30mg tablets, blister pack

arrotex pharmaceuticals pty ltd - gliclazide, quantity: 30 mg - tablet, modified release - excipient ingredients: hypromellose; stearic acid; colloidal anhydrous silica - type ii diabetes in association with dietary measures when dietary measures alone are inadequate to control blood glucose. during controlled clinical trials in patients with type ii diabetes, gliclazide mr 30 mg tablets, taken as a single daily dose, was shown to be effective long term in controlling blood glucose levels, based on monitoring of hba1c.

SILDENAFIL PHT ARX 20 mg sildenafil (as citrate) 20 mg film-coated tablets blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

sildenafil pht arx 20 mg sildenafil (as citrate) 20 mg film-coated tablets blister pack

accord healthcare pty ltd - sildenafil citrate, quantity: 28.1 mg (equivalent: sildenafil, qty 20 mg) - tablet, film coated - excipient ingredients: magnesium stearate; microcrystalline cellulose; hypromellose; croscarmellose sodium; calcium hydrogen phosphate; titanium dioxide; lactose monohydrate; triacetin - used to treat patients with pulmonary arterial hypertension classified as who functional classes ii and iii, to improve exercise capacity. efficacy has been shown in primary pulmonary hypertension and pulmonary hypertension associated with connective tissue disease. the efficacy of sildenafil citrate 20 mg has not been evaluated in patients currently on bosentan therapy.

ISOBIDE MR isosorbide mononitrate 60 mg modified release tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

isobide mr isosorbide mononitrate 60 mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - isosorbide mononitrate, quantity: 60 mg - tablet, modified release - excipient ingredients: hypromellose; carnauba wax; stearic acid; lactose monohydrate; magnesium stearate; purified talc; titanium dioxide; iron oxide yellow; macrogol 4000; colloidal anhydrous silica - prophylactic treatment of angina pectoris. isodur mr 60mg sustained release tablets are not recommended for the management of acute attacks of angina pectoris.

RIAMET artemether/lumefantrine 20 mg/120 mg tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

riamet artemether/lumefantrine 20 mg/120 mg tablet blister pack

novartis pharmaceuticals australia pty ltd - lumefantrine, quantity: 120 mg; artemether, quantity: 20 mg - tablet, uncoated - excipient ingredients: magnesium stearate; microcrystalline cellulose; colloidal anhydrous silica; polysorbate 80; croscarmellose sodium; hypromellose - riamet tablet is indicated for the treatment of acute, uncomplicated malaria due to plasmodium falciparum in adults, children and infants of 5kg and above. riamet is indicated for the treatment of acute, uncomplicated malaria due to plasmodium falciparum in patients aged at least 12 years and weighing at least 35kg.

APO-ISOSORBIDE MONONITRATE 60 mg modified release tablet blister pack Australien - engelska - Department of Health (Therapeutic Goods Administration)

apo-isosorbide mononitrate 60 mg modified release tablet blister pack

arrotex pharmaceuticals pty ltd - isosorbide mononitrate, quantity: 60 mg - tablet, modified release - excipient ingredients: purified talc; titanium dioxide; lactose monohydrate; hypromellose; stearic acid; magnesium stearate; iron oxide yellow; macrogol 4000; carnauba wax; colloidal anhydrous silica - prophylactic treatment of angina pectoris. apo- isosorbide mononitrate 60mg sustained release tablets are not recommended for the management of acute attacks of angina pectoris (see precautions).