Product image of Methadone Hydrochloride Inn-Farm (Methadone Hydrochloride) supplied by GNH India

Methadone Hydrochloride Inn-Farm

Active Ingredient:
Methadone Hydrochloride
Origin:
EU

Methadone Hydrochloride Inn-Farm (Methadone Hydrochloride)

Methadone Hydrochloride, the active ingredient in Methadone Hydrochloride Inn-Farm, is a synthetic opioid analgesic presented as an oral formulation for oral use. It is employed in the treatment of opioid dependence and for management of severe chronic pain in adult patients under medical supervision and requires careful dosing by qualified healthcare professionals.

GNH India supplies Methadone Hydrochloride Inn-Farm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide with robust quality assurance and regulatory compliance across multiple regions.

Manufacturer / TM Owner

Inn-Farm D.O.O.

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Indications & Clinical Uses

Methadone Hydrochloride is used in opioid‑related disorders and chronic pain management.

  • Opioid dependence (maintenance therapy): reduces withdrawal symptoms and cravings, supporting long‑term abstinence.
  • Severe chronic pain: provides long‑acting analgesia for patients requiring opioid therapy.
  • Opioid detoxification: facilitates supervised withdrawal by stabilizing opioid receptors.

How It Works

  • Methadone Hydrochloride acts as a full agonist at the µ‑opioid receptor, producing analgesia and suppressing withdrawal by activating the same pathways as endogenous opioids. It also blocks NMDA receptors and inhibits reuptake of serotonin and norepinephrine, contributing to its efficacy in pain modulation and reducing opioid tolerance. These combined actions result in a long‑lasting effect that supports maintenance therapy and chronic pain control.

Side Effects

Methadone Hydrochloride may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Constipation: reduced gastrointestinal motility leading to infrequent stools.
  • Nausea: feeling of sickness that may accompany oral intake.
  • Drowsiness: increased sleepiness affecting daily activities.
  • Sweating: excessive perspiration, especially at night.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing that can be life‑threatening.
  • QT interval prolongation: cardiac electrical disturbance increasing arrhythmia risk.
  • Severe hypotension: marked drop in blood pressure causing dizziness or fainting.

Precautions & Warnings

When prescribing Methadone Hydrochloride, clinicians should observe several safety measures to minimize risk.

  • Assess opioid tolerance: confirm the patient has prior exposure to opioids before initiating therapy.
  • Monitor respiratory function: observe for signs of depression, especially during dose adjustments.
  • Avoid use in acute severe asthma: methadone may exacerbate bronchospasm.
  • Use caution in hepatic impairment: liver disease can alter drug metabolism and increase plasma levels.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Methadone Hydrochloride interacts with several medications; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Concomitant CNS depressants: additive effect on respiratory depression and sedation.
  • QT‑prolonging agents: combined risk of cardiac arrhythmias.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole): may raise methadone plasma concentrations.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): can lower methadone levels and reduce efficacy.
  • Selective serotonin reuptake inhibitors: increase risk of serotonin syndrome when combined.

Frequently Asked Questions

Methadone Hydrochloride Inn-Farm is prescribed for opioid dependence maintenance therapy and for the management of severe chronic pain in adult patients. It helps reduce withdrawal symptoms, cravings, and provides long‑acting analgesia when other opioid treatments are required.

Methadone acts as a full agonist at the µ‑opioid receptor, mimicking the effects of endogenous opioids to relieve pain and suppress withdrawal. It also blocks NMDA receptors and inhibits serotonin and norepinephrine reuptake, which contributes to its ability to reduce opioid tolerance and improve pain control.

Dosing of Methadone Hydrochloride is individualized. The prescribing clinician determines the appropriate dose based on the patient’s opioid tolerance, clinical condition, and response to therapy. No standard dose is provided here; the prescriber tailors the regimen to each patient’s needs.

Methadone Hydrochloride is classified as Pregnancy Category C, indicating that risk cannot be ruled out. It may be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Methadone does pass into breast milk; breastfeeding decisions should be made in consultation with a healthcare professional.

To order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After submission, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details and any required import documentation.

The primary alternative is buprenorphine, a partial µ‑opioid receptor agonist. Methadone is a full agonist, offering more potent analgesia and a longer half‑life, which can be advantageous for severe dependence or chronic pain. Buprenorphine has a ceiling effect on respiratory depression, making it safer in overdose situations, but may be less effective for high‑level opioid tolerance.

Methadone Hydrochloride should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed to maintain stability throughout its shelf life.

Methadone Hydrochloride is administered orally. The exact dosage form (tablet, capsule, or liquid) is determined by the manufacturer, but the route of administration is by mouth, with the dose taken as directed by the prescribing clinician.

The most serious risks include respiratory depression, which can be life‑threatening, QT interval prolongation that may lead to cardiac arrhythmias, and severe hypotension. Patients should be monitored closely for signs of these events, especially during dose initiation or adjustment.

Methadone should be avoided in individuals with known hypersensitivity to the drug, those with acute severe asthma, uncontrolled cardiac arrhythmias, or significant respiratory compromise. It is also contraindicated in patients who have not previously been exposed to opioids without careful medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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