Malta - inglise - Medicines Authority

glaxosmithkline consumer health-care uk trading limited - paracetamol; pseudoephedrine hydrochloride - film-coated tablet - paracetamol 500 mg; pseudoephedrine hydrochloride 30 mg - analgesics

Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

chiesi farmaceutici s.p.a. - beclometasone dipropionate anhydrous; formoterol fumarate dihydrate - pressurised inhalation, solution - 200/6 µg/µg - adrenergics in combination with corticosteroids or other drugs, excl. anticholinergics; formoterol and beclometasone

Malaisia - inglise - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

duopharma (m) sdn. bhd. - pseudoephedrine hydrochloride; triprolidine hydrochloride -

Malta - inglise - Medicines Authority

haleon hellas single member societe anonyme, under the distinctive title of haleon hellas, 274, kifissias ave, 15232 chalandri, athens, greece - paracetamol, pseudoephedrine hydrochloride - film-coated tablet - pseudoephedrine hydrochloride 30 mg paracetamol 500 mg - analgesics

Singapur - inglise - HSA (Health Sciences Authority)

teva pharmaceutical investments singapore pte. ltd. - budesonide (micronised); formoterol fumarate dihydrate (micronised) - powder, metered - budesonide (micronised) 160 mcg / inhalation; formoterol fumarate dihydrate (micronised) 4.5 mcg / inhalation

Singapur - inglise - HSA (Health Sciences Authority)

teva pharmaceutical investments singapore pte. ltd. - budesonide (micronised); formoterol fumarate dihydrate (micronised) - powder, metered - budesonide (micronised) 320 mcg / inhalation; formoterol fumarate dihydrate (micronised) 9 mcg / inhalation

Lõuna-Aafrika Vabariik - inglise - South African Health Products Regulatory Authority (SAHPRA)

ranbaxy (sa) (pty) ltd - solution - see ingredients - each 5 ml solution contains codeine phosphate 7,5 mg guaifenesin 100 mg pseudoephedrine hydrochloride 20 mg triprolidine hydrochloride 1,25 mg

Lõuna-Aafrika Vabariik - inglise - South African Health Products Regulatory Authority (SAHPRA)

ranbaxy (sa) (pty) ltd - solution - see ingredients - each 5 ml solution contains codeine phosphate 3 mg guaifenesin 50 mg pseudoephedrine hydrochloride 12 mg triprolidine hydrochloride 0,6 mg

Lõuna-Aafrika Vabariik - inglise - South African Health Products Regulatory Authority (SAHPRA)

pharmacare limited û woodmead - solution - see ingredients - each 5 ml solution contains codeine phosphate 3 mg guaifenesin 50 mg pseudoephedrine hydrochloride 12 mg triprolidine hydrochloride 0,6 mg

Uus-Meremaa - inglise - Medsafe (Medicines Safety Authority)

boucher & muir (nz) ltd t/a mercury pharma (nz) - tranylcypromine sulfate 13.68mg equivalent to 10 mg tranylcypromine; tranylcypromine sulfate 13.68mg equivalent to 10 mg tranylcypromine - film coated tablet - 10 mg - active: tranylcypromine sulfate 13.68mg equivalent to 10 mg tranylcypromine excipient: calcium sulfate carnauba wax red spectraspray acsl0673 erythrosine gelatin hypromellose magnesium stearate maize starch propylene glycol shellac sucrose active: tranylcypromine sulfate 13.68mg equivalent to 10 mg tranylcypromine excipient: calcium sulfate carnauba wax erythrosine gelatin magnesium stearate maize starch opadry red 06h250000 sucrose - parnate is indicated for the treatment of symptoms of depressive illness especially where treatment with other types of anti-depressants has failed. it is not recommended for use in mild depressive states resulting from temporary situational difficulties.