Targin 80 mg/40 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

targin 80 mg/40 mg prolonged-release tablets

mundipharma pharmaceuticals limited - oxycodone hydrochloride; naloxone hydrochloride - prolonged-release tablet - 80 mg/40 milligram(s) - natural opium alkaloids; oxycodone, combinations

Naloxone Hydrochloride Hameln New Zealand - English - Medsafe (Medicines Safety Authority)

naloxone hydrochloride hameln

max health limited - naloxone hydrochloride dihydrate 0.44 mg/ml equivalent to 0.40 mg naloxone hydrochloride - solution for injection - 400 mcg/ml - active: naloxone hydrochloride dihydrate 0.44 mg/ml equivalent to 0.40 mg naloxone hydrochloride excipient: hydrochloric acid sodium chloride water for injection - naloxone hydrochloride injection is indicated for the complete or partial reversal of narcotic depression, including respiratory depression, induced by opioids including natural and synthetic narcotics, propoxyphene, methadone and the narcotic antagonist analgesics: nalbuphine, pentazocine and butorphanol. naloxone hydrochloride is also indicated for the diagnosis of suspected acute opioid overdosage.

Armoneve 40 mg/20 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

armoneve 40 mg/20 mg prolonged-release tablets

mundipharma pharmaceuticals limited - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 40/20 mg/mg - natural opium alkaloids; oxycodone, combinations

Armoneve 30 mg/15 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

armoneve 30 mg/15 mg prolonged-release tablets

mundipharma pharmaceuticals limited - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 30/15 mg/mg - natural opium alkaloids; oxycodone, combinations

Armoneve 20 mg/10 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

armoneve 20 mg/10 mg prolonged-release tablets

mundipharma pharmaceuticals limited - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 20/10 mg/mg - natural opium alkaloids; oxycodone, combinations

Armoneve 10 mg/5 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

armoneve 10 mg/5 mg prolonged-release tablets

mundipharma pharmaceuticals limited - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 10/5 mg/mg - natural opium alkaloids; oxycodone, combinations

Nolxado 10 mg/5 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nolxado 10 mg/5 mg prolonged-release tablets

krka, d.d., novo mesto - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 10 mg/ 5 milligram(s) - natural opium alkaloids; oxycodone, combinations

Nolxado 20 mg/10 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nolxado 20 mg/10 mg prolonged-release tablets

krka, d.d., novo mesto - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 20mg/10 milligram(s) - natural opium alkaloids; oxycodone, combinations

Nolxado 40 mg/20 mg prolonged-release tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nolxado 40 mg/20 mg prolonged-release tablets

krka, d.d., novo mesto - oxycodone hydrochloride; naloxone hydrochloride dihydrate - prolonged-release tablet - 40mg / 20 milligram(s) - natural opium alkaloids; oxycodone, combinations

Oxycodone/Naloxone Sandoz 20 mg - 10 mg tabl. prol.-rel. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

oxycodone/naloxone sandoz 20 mg - 10 mg tabl. prol.-rel.

sandoz sa-nv - oxycodone hydrochloride 20 mg; naloxone hydrochloride dihydrate 10,9 mg - eq. naloxone hydrochloride 10 mg - prolonged-release tablet - 20 mg - 10 mg - oxycodone hydrochloride 20 mg; naloxone hydrochloride dihydrate 10.9 mg - oxycodone, combinations