Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

renata limited - zafirlukast - tablet - 20 mg

Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

square pharmaceuticals plc, pabna - zafirlukast - tablet - 20 mg

Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

techno drugs ltd. - zafirlukast - tablet - 20 mg

Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

the acme laboratories ltd. - zafirlukast - tablet - 20 mg

Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

unimed unihealth pharmaceuticals ltd. - zafirlukast - tablet - 20 mg

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

zafirlukast -

Nový Zéland - angličtina - Medsafe (Medicines Safety Authority)

astrazeneca limited - zafirlukast 40mg;  ;   - tablet - 40 mg - active: zafirlukast 40mg     excipient: croscarmellose sodium hypromellose lactose monohydrate magnesium stearate microcrystalline cellulose povidone purified water   titanium dioxide

Irsko - angličtina - HPRA (Health Products Regulatory Authority)

b & s healthcare - zafirlukast - film coated tablet - 20 milligram

Bangladéš - angličtina - DGDA (Directorate General of Drug Administration)

square pharmaceuticals plc, pabna - zafirlukast - tablet - 10 mg

Kanada - angličtina - Health Canada

pharmaxis ltd - mannitol; mannitol; mannitol; mannitol - kit - 5mg; 10mg; 20mg; 40mg - mannitol 5mg; mannitol 10mg; mannitol 20mg; mannitol 40mg - diagnostic agents