Israel - English - Ministry of Health

rafa laboratories ltd - naloxone hydrochloride (as dihydrate); oxycodone hydrochloride - tablets prolonged release - naloxone hydrochloride (as dihydrate) 15 mg; oxycodone hydrochloride 30 mg - oxycodone and naloxone - targin is indicated for the relief of moderate to severe pain.the oxycodone component is indicated for the relief of moderate to severe pain in adults who require continuous around the- clock opioid analgesia for several days or more. the opioid antagonist naloxone is added to counteract opioid-induced constipation by blocking the action of oxycodone at opioid receptors locally in the gut.

Singapore - English - HSA (Health Sciences Authority)

dksh singapore pte. ltd. - naloxone 4.50mg eqv to naloxone hydrochloride anhydrous; oxycodone 9.00mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - 5.00 mg/tablet - naloxone 4.50mg eqv to naloxone hydrochloride anhydrous 5 mg; oxycodone 9.00mg eqv oxycodone hydrochloride anhydrous 10 mg

Singapore - English - HSA (Health Sciences Authority)

mundipharma pharmaceuticals pte. ltd. - naloxone 9.00mg eqv naloxone hydrochloride anhydrous; oxycodone 18.00mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - 10.00 mg/tablet - naloxone 9.00mg eqv naloxone hydrochloride anhydrous 10 mg; oxycodone 18.00mg eqv oxycodone hydrochloride anhydrous 20 mg

Singapore - English - HSA (Health Sciences Authority)

mundipharma pharmaceuticals pte. ltd. - naloxone 18.00mg eqv naloxone hydrochloride anhydrous; oxycodone 36.00mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - 20.00 mg/tablet - naloxone 18.00mg eqv naloxone hydrochloride anhydrous 20 mg; oxycodone 36.00mg eqv oxycodone hydrochloride anhydrous 40 mg

Singapore - English - HSA (Health Sciences Authority)

dksh singapore pte. ltd. - naloxone 2.25mg eqv naloxone hydrochloride anhydrous; oxycodone 4.50mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - 2.50 mg/tablet - naloxone 2.25mg eqv naloxone hydrochloride anhydrous 2.5 mg; oxycodone 4.50mg eqv oxycodone hydrochloride anhydrous 5 mg

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

napp pharmaceuticals ltd - oxycodone hydrochloride; naloxone hydrochloride - modified-release tablet - 5mg ; 2.5mg

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

napp pharmaceuticals ltd - oxycodone hydrochloride; naloxone hydrochloride - modified-release tablet - 40mg ; 20mg

Singapore - English - HSA (Health Sciences Authority)

mundipharma pharmaceuticals pte. ltd. - naloxone 27.00mg eqv naloxone hydrochloride anhydrous; oxycodone 54.00mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - naloxone 27.00mg eqv naloxone hydrochloride anhydrous 30.00mg; oxycodone 54.00mg eqv oxycodone hydrochloride anhydrous 60.00mg

Singapore - English - HSA (Health Sciences Authority)

mundipharma pharmaceuticals pte. ltd. - naloxone 36.00mg eqv naloxone hydrochloride anyhydrous; oxycodone 72.00mg eqv oxycodone hydrochloride anhydrous - tablet, film coated, extended release - naloxone 36.00mg eqv naloxone hydrochloride anyhydrous 40.00mg; oxycodone 72.00mg eqv oxycodone hydrochloride anhydrous 80.00mg

Ireland - English - HPRA (Health Products Regulatory Authority)

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