أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - metformin hydrochloride -

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - pseudoephedrine hydrochloride, quantity: 30 mg; dextromethorphan hydrobromide monohydrate, quantity: 15 mg; paracetamol, quantity: 500 mg - tablet, film coated - excipient ingredients: carnauba wax; purified water; povidone; magnesium stearate; hydrogenated vegetable oil; croscarmellose sodium; microcrystalline cellulose; pregelatinised maize starch; sodium starch glycollate; titanium dioxide; hypromellose; iron oxide yellow; macrogol 400 - provides temporary relief of nagging cough and discomfort associated with cold and flu: relieves blocked noses, dries runny noses, provides temporary relief of cough and headache, relieves body aches and pains, reduces fever.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - paracetamol, quantity: 500 mg; pseudoephedrine hydrochloride, quantity: 30 mg; chlorphenamine maleate, quantity: 2 mg - tablet, film coated - excipient ingredients: hydrogenated vegetable oil; croscarmellose sodium; pregelatinised maize starch; carnauba wax; magnesium stearate; microcrystalline cellulose; povidone; titanium dioxide; indigo carmine; hyprolose; iron oxide red; iron oxide black - provides fast and effective relief from the symptoms of cold and flu. the non-drowsy day tablet temporarily relieves: blocked noses, runny noses, nagging cough, headaches, body aches and pains, and fever. the night tablet contains an antihistamine and temporarily relieves: blocked noses, headaches, body aches and pains, and fever.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - codeine phosphate -

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharmacare australia pty ltd - dexamfetamine sulfate, quantity: 5 mg - tablet, uncoated - excipient ingredients: povidone; wheat starch; magnesium stearate; lactose monohydrate - indications as at 22 january 1997: narcolepsy and hyperkinetic behaviour disorders in children.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - prednisolone sodium phosphate, quantity: 0.27 mg/ml (equivalent: prednisolone, qty 0.2 mg/ml) - enema - excipient ingredients: purified water; isobutyl hydroxybenzoate; dibasic sodium phosphate heptahydrate; propyl hydroxybenzoate; ethyl hydroxybenzoate; sodium hydroxide; disodium edetate; methyl hydroxybenzoate; monobasic sodium phosphate; butyl hydroxybenzoate - predsol retention enema provides local corticosteroid treatment for rectal and rectosigmoidal disease in ulcerative colitis and crohn?s disease.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

arrow pharma pty ltd - esomeprazole magnesium dihydrate -

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

arrow pharma pty ltd - esomeprazole magnesium dihydrate -

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

kingsley healthcare pharmaceuticals pty ltd - aloes cape,benzoin sumatra,storax prepared -

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - lamotrigine, quantity: 200 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; croscarmellose sodium; colloidal anhydrous silica; povidone; saccharin sodium; purified talc; magnesium stearate; mannitol; flavour - seaze is an antiepileptic drug for the treatment of partial and generalised seizures in adults and children. there is extensive experience with lamotrigine used initially as add-on therapy. the use of lamotrigine has also been found to be effective as monotherapy following withdrawal of concomitant antiepileptic drugs. initial monotherapy therapy in newly diagnosed paediatric patients is not recommended.( see pharmacology, clinical trials.)