Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: hypromellose; sodium starch glycollate type a; microcrystalline cellulose; colloidal anhydrous silica; titanium dioxide; purified talc; maize starch; magnesium stearate; povidone; macrogol 6000; pregelatinised maize starch - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. gxp paracetamol xr 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: colloidal anhydrous silica; povidone; sodium starch glycollate type a; microcrystalline cellulose; magnesium stearate; titanium dioxide; purified talc; macrogol 6000; maize starch; pregelatinised maize starch; hypromellose - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. pharmacy choice osteo relief paracetamol 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: hypromellose; povidone; macrogol 6000; purified talc; maize starch; sodium starch glycollate type a; pregelatinised maize starch; microcrystalline cellulose; colloidal anhydrous silica; magnesium stearate; titanium dioxide - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. terry white chemists osteo relief paracetamol 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: purified talc; titanium dioxide; povidone; pregelatinised maize starch; hypromellose; microcrystalline cellulose; macrogol 6000; maize starch; magnesium stearate; colloidal anhydrous silica; sodium starch glycollate type a - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. chemmart pharmacy osteo relief paracetamol 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: purified talc; titanium dioxide; sodium starch glycollate type a; microcrystalline cellulose; povidone; colloidal anhydrous silica; magnesium stearate; maize starch; macrogol 6000; hypromellose; pregelatinised maize starch - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. ah paracetamol xr 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: macrogol 6000; colloidal anhydrous silica; magnesium stearate; titanium dioxide; microcrystalline cellulose; povidone; hypromellose; purified talc; maize starch; pregelatinised maize starch; sodium starch glycollate type a - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. gxp paracetamol xr 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Австралия - английский - Department of Health (Therapeutic Goods Administration)

neo health (otc) pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: sodium starch glycollate type a; macrogol 6000; hypromellose; titanium dioxide; maize starch; magnesium stearate; colloidal anhydrous silica; povidone; pregelatinised maize starch; purified talc; microcrystalline cellulose - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. genpar paracetamol xr 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Бельгия - английский - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

air liquide santé international s.a. - xenon 100 % - medicinal gas, liquefied - xenon - xenon

Австралия - английский - Department of Health (Therapeutic Goods Administration)

ucb australia pty ltd t/a ucb pharma division of ucb australia - brivaracetam, quantity: 10 mg/ml - oral liquid, solution - excipient ingredients: sodium citrate dihydrate; purified water; methyl hydroxybenzoate; citric acid; glycerol; carmellose sodium; sorbitol solution (70 per cent) (crystallising); sucralose; flavour - briviact oral solution is indicated as add-on therapy in the treatment of partial onset seizures with or without secondary generalisation in patients from 4 years of age with epilepsy

Австралия - английский - Department of Health (Therapeutic Goods Administration)

ucb australia pty ltd t/a ucb pharma division of ucb australia - levetiracetam, quantity: 100 mg/ml - oral liquid, solution - excipient ingredients: acesulfame potassium; purified water; maltitol solution; methyl hydroxybenzoate; ammonium glycyrrhizinate; citric acid monohydrate; propyl hydroxybenzoate; sodium citrate dihydrate; glycerol; flavour - keppra (film coated tablets and oral solution) is indicated for - use in epileptic patients aged 4 years and older, initially as add-on therapy, in the treatment of partial onset seizures with or without secondary generalisation, - monotherapy in the treatment of partial onset seizures, with or without secondary generalisation, in patients from 16 years of age with newly diagnosed epilepsy. - add on therapy in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy (jme), and - add on therapy in the treatment of primary generalised tonic-clonic seizures in adults and children from 4 years of age with idiopathic generalised epilepsy (ige). keppra concentrate solution for iv infusion after dilution is an alternative for patients when oral administration is temporarily not feasible.