Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 30 mg - tablet, uncoated - excipient ingredients: potassium sorbate; maize starch; povidone; purified talc; stearic acid; magnesium stearate; microcrystalline cellulose; croscarmellose sodium; pregelatinised maize starch - paracetamol/codeine gh 500/30 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.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - codeine phosphate hemihydrate, quantity: 9.6 mg; paracetamol, quantity: 500 mg - tablet, uncoated - excipient ingredients: sodium starch glycollate; magnesium stearate; purified talc; stearic acid; povidone; pregelatinised maize starch; crospovidone - for the relief of acute moderate pain and fever

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

generic health pty ltd - codeine phosphate hemihydrate, quantity: 15 mg; paracetamol, quantity: 500 mg - tablet, uncoated - excipient ingredients: magnesium stearate; colloidal anhydrous silica; lactose monohydrate; docusate sodium; povidone; potato starch - for the relief of acute moderate pain and fever.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

soul pattinson manufacturing pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 10 mg; doxylamine succinate, quantity: 5.1 mg - tablet, uncoated - excipient ingredients: stearic acid; magnesium stearate; ethanol; microcrystalline cellulose; lactose monohydrate; maize starch; povidone; crospovidone - for the temporary relief of acute moderate pain and fever.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - codeine phosphate hemihydrate, quantity: 9.75 mg; doxylamine succinate, quantity: 5 mg; paracetamol, quantity: 450 mg - tablet, uncoated - excipient ingredients: magnesium stearate; purified talc; microcrystalline cellulose; sodium starch glycollate; quinoline yellow; sunset yellow fcf; stearic acid; povidone; pregelatinised maize starch; crospovidone - for the relief of acute moderate pain and fever

Malta - enska - Medicines Authority

reckitt benckiser ireland ltd 7 riverwalk citywest business campus dublin 24 , ireland - ibuprofen, codeine phosphate, hemihydrate - film-coated tablet - ibuprofen 200 mg codeine phosphate hemihydrate 12.8 mg - analgesics

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

apotex pty ltd - codeine phosphate hemihydrate,doxylamine succinate,paracetamol -

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

apotex pty ltd - codeine phosphate hemihydrate,doxylamine succinate,paracetamol -

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

apotex pty ltd - codeine phosphate hemihydrate,doxylamine succinate,paracetamol -

Írland - enska - HPRA (Health Products Regulatory Authority)

imbat limited - codeine phosphate hemihydrate; ibuprofen - film-coated tablet - 200 mg/12.8 milligram(s) - opioids in combination with non-opioid analgesics; codeine and ibuprofen