PHARMACY ACTION PARACETAMOL OSTEO 665 paracetamol 665 mg modified release tablet blister pack Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

pharmacy action paracetamol osteo 665 paracetamol 665 mg modified release tablet blister pack

lupin australia pty limited - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: hypromellose; magnesium stearate; microcrystalline cellulose; silicon dioxide; povidone; pregelatinised maize starch; purified water; croscarmellose sodium; titanium dioxide; macrogol 6000 - pharmacy action paracetamol osteo provides effective relief from persistent pain for up to 8 hours. effective for the relief of persistent pain associated with osteoarthritis and muscular aches and pains such as backache. provides effective temporary relief of pain and discomfort associated with: headache, tension headache, cold and flu, period pain, toothache and pain after dental procedures. reduces fever.

FEBRICOL TABLETS 500MG / 30MG /2MG ORAL SOLID ORDINARY TABLETS Uganda - angol - National Drug Authority

febricol tablets 500mg / 30mg /2mg oral solid ordinary tablets

xepa soul pattison (m) sdn bhd - paracetamol / pseudoephedrine / chlorpheniramine - oral solid ordinary tablets - 500mg / 30mg /2mg

AUGMENTIN DUO 400 powder for oral liquid bottle Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

augmentin duo 400 powder for oral liquid bottle

aspen pharmacare australia pty ltd - clavulanic acid, quantity: 11.4 mg/ml; amoxicillin, quantity: 80 mg/ml - oral liquid, powder for - excipient ingredients: silicon dioxide; succinic acid; colloidal anhydrous silica; aspartame; xanthan gum; hypromellose; flavour - augmentin duo 400 oral suspension is indicated in the short term treatment of the following bacterial infections when caused by sensitive organisms (see microbiology). skin and skin structure infections: urinary tract infections (complicated and uncomplicated): upper respiratory tract infections including sinusitis, otitis media: lower respiratory tract infections including acute exacerbations of chronic bronchitis and community acquired pneumonia. appropriate culture and susceptibility studies should be performed to identify the causative organism(s) and determine its (their) susceptibility to augmentin. however, when there is good reason to believe an infection may involve any of the beta-lactamase producing organisms listed above, therapy may be instituted prior to obtaining the results from bacteriological and susceptible studies. once these results are known, therapy should be adjusted if appropriate. the treatment of mixed infections caused by amoxycillin susceptible organisms and beta-lactamase producing organisms susceptible to augmentin duo 400, should not require the addition of another antibiotic due to the amoxycillin content of augmentin duo 400.

Paracetamol Krka 500 mg tablets Írország - angol - HPRA (Health Products Regulatory Authority)

paracetamol krka 500 mg tablets

krka, d.d., novo mesto - paracetamol - tablet - 500 milligram(s) - paracetamol

Paracetamol Tablets Effervescent 500mg Málta - angol - Medicines Authority

paracetamol tablets effervescent 500mg

cipla (eu) limited hillbrow house, hillbrow road, esher, surrey, kt10 9nw, united kingdom - paracetamol - effervescent tablet - paracetamol 500 mg - analgesics

PARACETAMOL OSTEO-TAB paracetamol 665 mg modified release tablet bottle Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

paracetamol osteo-tab paracetamol 665 mg modified release tablet bottle

aft pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: magnesium stearate; purified water; microcrystalline cellulose; pregelatinised maize starch; hypromellose; croscarmellose sodium; povidone; titanium dioxide; lactose monohydrate; macrogol 3000 - for the relief of persistent pain associated with osteoarthritis.

Paracetamol Osteo-Tab paracetamol 665 mg modified release tablet blister pack Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

paracetamol osteo-tab paracetamol 665 mg modified release tablet blister pack

aft pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: purified water; magnesium stearate; pregelatinised maize starch; hypromellose; microcrystalline cellulose; croscarmellose sodium; povidone; titanium dioxide; lactose monohydrate; macrogol 3000 - for the relief of persistent pain associated with osteoarthritis.

PARACETAMOL GENPAR 500 mg film coated tablet blister pack Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

paracetamol genpar 500 mg film coated tablet blister pack

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 500 mg - tablet, film coated - excipient ingredients: maize starch; methyl hydroxybenzoate; microcrystalline cellulose; magnesium stearate; propyl hydroxybenzoate; povidone; croscarmellose sodium; crospovidone; purified talc; colloidal anhydrous silica; titanium dioxide; lactose monohydrate; hypromellose; triacetin - temporary relief of pain associated with headache, migraine headache, tension headache, sinus pain, toothache, dental procedures, backache, muscular aches and pains, arthritis, osteoarthritis, rheumatic pain, period pain, fibrositis, neuralgia, sore throat, tennis elbow, and colds and flu. reduces fever.