澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

mundipharma pty ltd - oxycodone hydrochloride, quantity: 10 mg; naloxone hydrochloride dihydrate, quantity: 5.45 mg (equivalent: naloxone hydrochloride?, qty 5 mg) - tablet, modified release - excipient ingredients: titanium dioxide; lactose monohydrate; stearyl alcohol; macrogol 3350; ethylcellulose; polyvinyl alcohol; purified talc; magnesium stearate; povidone - targin modified release tablet is indicated for the management of severe pain where:,- other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and,- the pain is opioid-responsive; and,- requires daily, continuous, long term treatment.,targin modified release tablet is not indicated for use in chronic non-cancer pain other than in exceptional circumstances.,targin modified release tablet is not indicated as an as-needed (prn) analgesia,the naloxone component in a fixed combination with oxycodone is indicated for the therapy and/or prophylaxis of opioid-induced constipation.,targin is indicated as a second line symptomatic treatment of patients with severe to very severe idiopathic restless legs syndrome after failure of dopaminergic therapy.

澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

mundipharma pty ltd - oxycodone hydrochloride, quantity: 5 mg; naloxone hydrochloride dihydrate, quantity: 2.73 mg (equivalent: naloxone hydrochloride?, qty 2.5 mg) - tablet, modified release - excipient ingredients: ethylcellulose; macrogol 3350; brilliant blue fcf aluminium lake; stearyl alcohol; polyvinyl alcohol; titanium dioxide; magnesium stearate; lactose monohydrate; purified talc; hyprolose - targin modified release tablet is indicated for the management of severe pain where:,- other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and,- the pain is opioid-responsive; and,- requires daily, continuous, long term treatment.,targin modified release tablet is not indicated for use in chronic non-cancer pain other than in exceptional circumstances.,targin modified release tablet is not indicated as an as-needed (prn) analgesia,the naloxone component in a fixed combination with oxycodone is indicated for the therapy and/or prophylaxis of opioid-induced constipation.,targin is indicated as a second line symptomatic treatment of patients with severe to very severe idiopathic restless legs syndrome after failure of dopaminergic therapy.

以色列 - 英文 - Ministry of Health

teva israel ltd - pethidine hydrochloride - solution for injection - pethidine hydrochloride 50 mg/ml - pethidine - pethidine - relief of severe pain pre-operative medication support of anesthesia obstetrical analgesia.

澳大利亚 - 英文 - APVMA (Australian Pesticides and Veterinary Medicines Authority)

parnell - pethidine hcl(50mg/ml) - parenteral liquid/solution/suspension - analgesic,spasmolytic - cat | cat - small | cattle | dog | dog - small or toy | horse | beef | bitch | bos indicus | bos taurus | bovine | buffalo | bul - analgesic | cough suppression | pre-anaesthetic | spasmolytic | anaesthetic premedicant | antipyretic | bronchitis | bronchodilation | colic | cough suppressants | decongestants | expectorants | mucoid secretions | mucolytics | muscle relaxant | respiratory conditions | sedative | sinusitis | spasmolytic

纳米比亚 - 英文 - Namibia Medicines Regulatory Council

pharma - q holdings (pty) ltd - pethidine hydrochloride - injection - pethidine hydrochloride injection 50 mg/ml

纳米比亚 - 英文 - Namibia Medicines Regulatory Council

pharma - q holdings (pty) ltd - pethidine hydrochloride - injection - pethidine hydrochloride injection 100 mg/2ml

新加坡 - 英文 - HSA (Health Sciences Authority)

pfizer private limited - pethidine hcl - injection - 50 mg/ml - pethidine hcl 50 mg/ml

新加坡 - 英文 - HSA (Health Sciences Authority)

zyfas pharma pte ltd - pethidine 43.57mg as pethidine hydrochloride - injection, solution - 50mg - pethidine 43.57mg as pethidine hydrochloride 50mg

马来西亚 - 英文 - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

imeks pharma sdn. bhd. - pethidine hydrochloride -

孟加拉国 - 英文 - DGDA (Directorate General of Drug Administration)

gonoshasthaya pharmaceuticals ltd. - pethidine hydrochloride - injection - 50 mg/ml