Israel - English - Ministry of Health

perrigo israel agencies ltd - remifentanil as hydrochloride - powder for reconstitution for solution for injection - remifentanil as hydrochloride 2 mg/vial - remifentanil - remifentanil - ultiva is indicated as an analgesic agent for use during induction and/or maintenance of general anaesthesia under close supervision . ultiva is indicated for provision of analgesia and sedation in mechanically ventilated intensive care patients 18 years of age and over.

Australia - English - Department of Health (Therapeutic Goods Administration)

glaxosmithkline australia pty ltd - remifentanil hydrochloride -

New Zealand - English - Medsafe (Medicines Safety Authority)

pharmacy retailing (nz) ltd t/a healthcare logistics - remifentanil hydrochloride 1.1mg equivalent to 1 mg remifentanil;   - powder for injection - 1 mg - active: remifentanil hydrochloride 1.1mg equivalent to 1 mg remifentanil   excipient: glycine hydrochloric acid sodium hydroxide water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

pharmacy retailing (nz) ltd t/a healthcare logistics - remifentanil hydrochloride 2.2mg equivalent to 2 mg remifentanil;   - powder for injection - 2 mg - active: remifentanil hydrochloride 2.2mg equivalent to 2 mg remifentanil   excipient: glycine hydrochloric acid sodium hydroxide water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - remifentanil hydrochloride 5.5mg equivalent to 5 mg remifentanil - powder for injection - 5 mg - active: remifentanil hydrochloride 5.5mg equivalent to 5 mg remifentanil excipient: glycine hydrochloric acid sodium hydroxide water for injection

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - remifentanil hydrochloride - pdr/conc/soln for infus - 2 milligram - opioid anesthetics

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - remifentanil hydrochloride - pdr/conc/soln for infus - 1 milligram - opioid anesthetics

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - remifentanil hydrochloride - pdr/conc/soln for infus - 5 milligram - opioid anesthetics

Singapore - English - HSA (Health Sciences Authority)

dch auriga singapore - remifentanil hydrochloride eqv remifentanil - injection, powder, for solution - 1 mg/vial - remifentanil hydrochloride eqv remifentanil 1 mg/vial

Malta - English - Medicines Authority

glaxo smithkline uk limited - remifentanil 2 mg - powder for solution for injection