Austrália - inglês - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - tramadol hydrochloride, quantity: 37.5 mg; paracetamol, quantity: 325 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; macrogol 8000; hypromellose; hyprolose; stearic acid; titanium dioxide; croscarmellose sodium; iron oxide yellow; pregelatinised maize starch; povidone - tramadol/paracetamol is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Irlanda - inglês - HPRA (Health Products Regulatory Authority)

paladin labs europe limited - tramadol hydrochloride paracetamol paracetamol - tablet prolonged release - 75/650 milligram

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - paracetamol, quantity: 1 g - injection, solution - excipient ingredients: glucose monohydrate; sodium citrate dihydrate; water for injections; glacial acetic acid; hydrochloric acid; sodium acetate trihydrate; sodium hydroxide - for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - paracetamol, quantity: 500 mg - injection, solution - excipient ingredients: hydrochloric acid; sodium citrate dihydrate; sodium acetate trihydrate; glucose monohydrate; sodium hydroxide; glacial acetic acid; water for injections - for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

Nova Zelândia - inglês - Medsafe (Medicines Safety Authority)

psm healthcare ltd trading as api consumer brands - paracetamol 500mg (as 556mg paracetamol dc90.);  ;  ; paracetamol 500mg (as 556mg of paracetamol dc90); paracetamol 500mg (as 556mg of paracetamol dc90) - tablet - 500 mg - active: paracetamol 500mg (as 556mg paracetamol dc90.)     paracetamol 500mg (as 556mg of paracetamol dc90) excipient: croscarmellose sodium as 556mg of paracetamol dc90 maize starch as 556mg of paracetamol dc90 povidone as 556mg of paracetamol dc90 stearic acid as 556mg of paracetamol dc90 active: paracetamol 500mg (as 556mg of paracetamol dc90) excipient: croscarmellose sodium as 556mg of paracetamol dc90 maize starch as 556mg of paracetamol dc90 povidone as 556mg of paracetamol dc90 stearic acid as 556mg of paracetamol dc90

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - paracetamol, quantity: 0.1 g - injection - excipient ingredients: water for injections; glacial acetic acid; mannitol; sodium citrate dihydrate - b. braun paracetamol 10 mg/ml, solution for infusion is indicated for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - paracetamol, quantity: 1 g - injection - excipient ingredients: water for injections; glacial acetic acid; sodium citrate dihydrate; mannitol - b. braun paracetamol 10 mg/ml, solution for infusion is indicated for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - paracetamol, quantity: 0.5 g - injection - excipient ingredients: water for injections; glacial acetic acid; mannitol; sodium citrate dihydrate - b. braun paracetamol 10 mg/ml, solution for infusion is indicated for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

Irlanda - inglês - HPRA (Health Products Regulatory Authority)

krka, d.d., novo mesto - paracetamol; tramadol hydrochloride - film-coated tablet - 37.5 mg/325 milligram(s) - opioids in combination with non-opioid analgesics; opiods in combination with non-opiod analgesics

Austrália - inglês - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 30 mg - tablet - excipient ingredients: magnesium stearate; stearic acid; povidone; pregelatinised maize starch - short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.