United States - English - NLM (National Library of Medicine)

h.j. harkins company inc. - methadone hydrochloride (unii: 229809935b) (methadone - unii:uc6vbe7v1z) - methadone hydrochloride 5 mg - - for the treatment of moderate to severe pain not responsive to non-narcotic analgesics. - for detoxification treatment of opioid addiction (heroin or other morphine-like drugs). - for maintenance treatment of opioid addiction (heroin or other morphine-like drugs), in conjunction with appropriate social and medical services. note – outpatient maintenance and outpatient detoxification treatment may be provided only by opioid treatment programs (otps) certified by the federal substance abuse and mental health services administration (samhsa) and registered by the drug enforcement administration (dea). this does not preclude the maintenance treatment of a patient with concurrent opioid addiction who is hospitalized for conditions other than opioid addiction and who requires temporary maintenance during the critical period of his/her stay, or of a patient whose enrollment has been verified in a program which has been certified for maintenance treatment with methadone. methadone is contr

New Zealand - English - Medsafe (Medicines Safety Authority)

aft pharmaceuticals ltd - methadone hydrochloride 10mg - tablet - 10 mg - active: methadone hydrochloride 10mg excipient: lactose monohydrate magnesium stearate starch - methadone is indicated for relief of severe pain. methadone is sometimes used as an antitussive when severe pain is present, and coughing cannot be relieved by other means. methadone is not recommended for obstetric analgesia because its long duration of action increases the risk of neonatal respiratory depression.

New Zealand - English - Medsafe (Medicines Safety Authority)

aft pharmaceuticals ltd - methadone hydrochloride 5mg - tablet - 5 mg - active: methadone hydrochloride 5mg excipient: lactose monohydrate magnesium stearate starch - methadone is indicated for relief of severe pain. methadone is sometimes used as an antitussive when severe pain is present, and coughing cannot be relieved by other means. methadone is not recommended for obstetric analgesia because its long duration of action increases the risk of neonatal respiratory depression.

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

aft pharmaceuticals pty ltd - methadone hydrochloride, quantity: 5 mg - tablet - excipient ingredients: pregelatinised maize starch; lactose monohydrate; magnesium stearate - methadone-aft 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.,methadone-aft is not indicated for use in chronic non-cancer pain other than in exceptional circumstances.,methadone-aft is not indicated as an as-needed (prn) analgesia.,methadone-aft is not recommended for use in ambulant patients.

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

aft pharmaceuticals pty ltd - methadone hydrochloride, quantity: 10 mg - tablet - excipient ingredients: magnesium stearate; pregelatinised maize starch; lactose monohydrate - methadone-aft 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.,methadone-aft is not indicated for use in chronic non-cancer pain other than in exceptional circumstances.,methadone-aft is not indicated as an as-needed (prn) analgesia.,methadone-aft is not recommended for use in ambulant patients.

Armenia - English - Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

specgx llc - methadone (methadone hydrochloride) - tablets - 5mg

Armenia - English - Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

specgx llc - methadone (methadone hydrochloride) - tablets - 10mg

United States - English - NLM (National Library of Medicine)

bryant ranch prepack - methadone hydrochloride (unii: 229809935b) (methadone - unii:uc6vbe7v1z) - methadone hydrochloride tablets are indicated for the: 1.  management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate. limitations of use - because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses, and because of the greater risks of overdose and death with long-acting opioids, reserve methadone hydrochloride tablets for use in patients for whom alternative analgesic treatment options (e.g., non-opioid analgesics or immediate-release opioid analgesics) are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. - methadone hydrochloride tablets are not indicated as an as-needed (prn) analgesic. 2. detoxification treatment of opioid addiction (heroin or other morphine-like drugs). 3. maintenance treatment of opioid addiction (heroin or other morphine-like drugs), in conjunction with appropriate social and medical services.

United States - English - NLM (National Library of Medicine)

vistapharm, inc. - methadone hydrochloride (unii: 229809935b) (methadone - unii:uc6vbe7v1z) - methadone hydrochloride tablets for oral suspension, usp contain methadone, an opioid agonist indicated for the: - detoxification treatment of opioid addiction (heroin or other morphine-like drugs). - maintenance treatment of opioid addiction (heroin or other morphine-like drugs), in conjunction with appropriate social and medical services. limitations of use methadone products used for the treatment of opioid addiction in detoxification or maintenance programs are subject to the conditions for distribution and use required under 42 cfr 8.12 [see dosage and administration ( 2.1)] . methadone hydrochloride tablets for oral suspension are contraindicated in patients with: - significant respiratory depression [see warnings and precautions (5.1)] - acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment [see warnings and precautions (5.8)] - known or suspected gastrointestinal obstruction, including paralytic ileus [see warnings and precautions (5.13)] - hypersensit

New Zealand - English - Medsafe (Medicines Safety Authority)

boucher & muir (new zealand) limited t/a bnm group - methadone hydrochloride 5mg - tablet - 5 mg - active: methadone hydrochloride 5mg excipient: colloidal silicon dioxide lactose monohydrate magnesium stearate maize starch povidone purified talc - methadone is indicated for relief of severe pain. methadone is sometimes used as an antitussive when severe pain is present and coughing cannot be relieved by other means. methadone is not recommended for obstetric analgesia because its long duration of action increases the risk of neonatal respiratory depression.