Malta - English - Medicines Authority

actavis group ptc ehf revkjavikurvegi 76-78, 220 hafnarfjordur, iceland - ibuprofen - film-coated tablet - ibuprofen 200 mg - antiinflammatory and antirheumatic products

Malta - English - Medicines Authority

actavis group ptc ehf revkjavikurvegi 76-78, 220 hafnarfjordur, iceland - ibuprofen - film-coated tablet - ibuprofen 400 mg - antiinflammatory and antirheumatic products

Australia - English - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - voriconazole, quantity: 200 mg - tablet, film coated - excipient ingredients: pregelatinised maize starch; lactose monohydrate; povidone; croscarmellose sodium; magnesium stearate; titanium dioxide; hypromellose; triacetin - voriconazole sandoz is indicated for treatment of the following fungal infections:,- invasive aspergillosis.,- serious candida infections (including c. krusei), including oesophageal and systemic candida infections (hepatosplenic candidiasis, disseminated candidiasis, candidaemia).,- serious fungal infections caused by scedosporium spp and fusarium spp.,- other serious fungal infections, in patients intolerant of, or refractory to, other therapy,- prophylaxis in patients who are at high risk of developing invasive fungal infections. the indication is based on studies including patients undergoing haematopoietic stem cell transplantation.,- this brand is only available as tablets and therefore only indicated for adults and children 12 years or older who can tolerate tablets. for dosing requirements for populations who require intravenous or oral suspension treatment see dosage and administration.

Australia - English - Department of Health (Therapeutic Goods Administration)

cipla australia pty ltd - codeine phosphate hemihydrate, quantity: 12.8 mg; ibuprofen, quantity: 200 mg - tablet, film coated - excipient ingredients: glyceryl behenate; magnesium stearate; maize starch; lactose monohydrate; purified water; colloidal anhydrous silica; titanium dioxide; hypromellose; macrogol 6000 - cipla pain relief ibuprofen plus is used for temporary relief of acute moderate pain and inflammation

Ireland - English - HPRA (Health Products Regulatory Authority)

clonmel healthcare ltd - ibuprofen; phenylephrine hydrochloride - film-coated tablet - 400/10 milligram(s) - other cold preparations

Malta - English - Medicines Authority

mylan ire healthcare limited unit 35/36, grange parade, baldoyle industrial estate, dublin 13, ireland - ibuprofen - film-coated tablet - ibuprofen 400 mg - antiinflammatory and antirheumatic products

Malta - English - Medicines Authority

pharos – pharmaceutical oriented services limited lesvou str. (end), thesi loggos, industrial zone, 144 52 metamorfossi attikis,, greece - ibuprofen, paracetamol - film-coated tablet - ibuprofen 200 mg paracetamol 500 mg - antiinflammatory and antirheumatic products

Ireland - English - HPRA (Health Products Regulatory Authority)

bluefish pharmaceuticals ab - ibuprofen - film-coated tablet - ibuprofen

Ireland - English - HPRA (Health Products Regulatory Authority)

bluefish pharmaceuticals ab - ibuprofen - film-coated tablet - ibuprofen

Australia - English - Department of Health (Therapeutic Goods Administration)

viatris pty ltd - ibuprofen, quantity: 400 mg - tablet, film coated - excipient ingredients: titanium dioxide; macrogol 6000; croscarmellose sodium; purified water; povidone; sodium lauryl sulfate; stearic acid; colloidal anhydrous silica; lactose monohydrate; microcrystalline cellulose; purified talc; hypromellose - for the temporary relief of pain and/or inflammation associated with headache, migraine headache, tension headache, sinus pain, toothache, dental procedures, backache, muscular aches and pains, period pain, sore throat, tennis elbow, arthritis, rheumatic pain and aches and pains associated with colds and flu. reduces fever.