Irsko - angličtina - HPRA (Health Products Regulatory Authority)

eli lilly and company limited - methohexital sodium sodium carbonate anhydrous - pdr for soln for injection - 100 milligram

Irsko - angličtina - HPRA (Health Products Regulatory Authority)

eli lilly and company limited - pdr for soln for injection - 500 milligram

Irsko - angličtina - HPRA (Health Products Regulatory Authority)

eli lilly and company limited - methohexital sodium - 2.5 g/100ml

Irsko - angličtina - HPRA (Health Products Regulatory Authority)

eli lilly and company limited - methohexital sodium - 5 g/100ml

Irsko - angličtina - HPRA (Health Products Regulatory Authority)

eli lilly and company limited - methohexital sodium - 2.5 g/100ml

Nový Zéland - angličtina - Medsafe (Medicines Safety Authority)

eli lilly and company (nz) limited - methohexital sodium 500mg;   - powder for injection - 500 mg - active: methohexital sodium 500mg  

Nový Zéland - angličtina - Medsafe (Medicines Safety Authority)

eli lilly and company (nz) limited - methohexital sodium 500mg - solution for injection - 500 mg - active: methohexital sodium 500mg

Kanada - angličtina - Health Canada

eli lilly canada inc - methohexital sodium - powder for solution - 500mg - methohexital sodium 500mg - barbiturates

Saúdská Arábie - angličtina - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

eli lilly and company - methohexital sodium - powder for injection - 10 mg/ml

Jihoafrická republika - angličtina - South African Health Products Regulatory Authority (SAHPRA)

eli lilly (sa) (pty) ltd - injection - each vial contains methohexital sodium 100 mg