Product image of Methadone Martindale Pharma (Methadone Hydrochloride) supplied by GNH India

Methadone Martindale Pharma

Active Ingredient:
Methadone Hydrochloride
Origin:
EU

Methadone Martindale Pharma (Methadone Hydrochloride)

Methadone Hydrochloride, the active ingredient in Methadone Martindale Pharma, is an opioid presented as an oral formulation for oral use. It acts as a long‑acting opioid agonist to treat opioid dependence and to provide analgesia for chronic pain in adult patients.

GNH India supplies Methadone Martindale Pharma as a licensed, GMP‑qualified, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide under strict quality‑assurance standards. The company adheres to EU pharmacopoeial specifications and ensures secure logistics for global markets.

Manufacturer / TM Owner

Ethypharm

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Indications & Clinical Uses

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

  • Opioid dependence treatment: stabilizes patients on a long‑acting opioid to reduce cravings and withdrawal symptoms.
  • Opioid detoxification: facilitates gradual tapering of opioid use during supervised withdrawal programs.
  • Chronic pain management: provides sustained analgesia for severe, long‑term pain when other opioids are insufficient.

How It Works

  • Methadone Hydrochloride exerts its effect primarily as a full agonist at the µ‑opioid receptor, producing analgesia and suppressing withdrawal. It also antagonizes NMDA receptors and blocks sodium channels, which contributes to its efficacy in opioid dependence and reduces the development of tolerance. The combined actions result in prolonged receptor activation and modulation of pain pathways.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Constipation: reduced bowel movements.
  • Drowsiness: increased sleepiness or fatigue.
  • Sweating: excessive perspiration.
  • Dizziness: feeling light‑headed or unsteady.
  • Dry mouth: reduced salivation.
  • Headache: mild to moderate head pain.
  • Weight gain: increase in body weight.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Cardiac arrhythmia: QT interval prolongation leading to irregular heart rhythm.
  • Severe allergic reaction: rash, itching, swelling, or anaphylaxis.
  • Adrenal insufficiency: fatigue, low blood pressure, electrolyte imbalance.
  • Seizures: rare occurrence of convulsive episodes.

Precautions & Warnings

When using Methadone Hydrochloride, careful clinical monitoring is essential.

  • Dose titration: adjust dose gradually under medical supervision.
  • Monitoring: regular assessment of respiratory function and ECG.
  • Pregnancy: use only if benefits outweigh risks.
  • Concomitant CNS depressants: avoid or use with caution.
  • Driving: may impair ability; avoid operating machinery.
  • Renal/hepatic impairment: dose may need adjustment.
  • Store at ambient temperature below 25°C: keep in original container, protect from moisture and light.

Avoid Interactions

Methadone Hydrochloride interacts with several drug classes; clinicians should review patient medication lists.

Major Interactions (Avoid)

  • Concurrent use with other opioids or CNS depressants: risk of profound respiratory depression.
  • MAO inhibitors: can cause severe hypotension and serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): increase methadone plasma levels.
  • CYP3A4 inducers (e.g., rifampin): reduce methadone effectiveness.
  • Antiretrovirals (e.g., efavirenz): may lower methadone concentrations.

Frequently Asked Questions

Methadone Martindale Pharma contains methadone hydrochloride and is prescribed for the treatment of opioid dependence, including maintenance therapy and supervised detoxification, as well as for the management of severe chronic pain when other analgesics are inadequate.

Methadone hydrochloride acts as a full agonist at the µ‑opioid receptor, providing analgesia and suppressing withdrawal symptoms. It also blocks NMDA receptors and sodium channels, which helps reduce tolerance development and contributes to its effectiveness in opioid‑dependence programs.

The dose of methadone is individualized. A qualified prescriber determines the appropriate starting dose, titration schedule, and maintenance dose based on the patient’s clinical condition, prior opioid exposure, and response to therapy.

Data on methadone use during pregnancy and lactation are limited. It may be prescribed if the therapeutic benefit outweighs potential risks to the fetus or infant, but the decision should be made by a healthcare professional familiar with the patient’s obstetric history.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Both methadone and buprenorphine are opioid agonists used for dependence treatment. Methadone is a full µ‑opioid agonist offering stronger analgesia but requires more careful dosing and monitoring for respiratory depression. Buprenorphine is a partial agonist with a ceiling effect on respiratory depression, often considered safer for outpatient use, though it may be less effective for severe pain.

Store the product at ambient temperature below 25 °C, in its original packaging, protected from moisture and direct light. Keep out of reach of children and do not use if the packaging is damaged or the product appears discolored.

Methadone Martindale Pharma is administered orally. The tablet or oral solution should be swallowed whole with water as directed by the prescriber. Do not crush, split, or chew the dosage form unless specifically instructed.

The most serious risks include respiratory depression, especially when combined with other CNS depressants, and cardiac arrhythmias due to QT‑interval prolongation. Overdose can be life‑threatening, and rare allergic reactions such as anaphylaxis may occur.

Methadone should be avoided in individuals with known hypersensitivity to methadone, severe uncontrolled asthma, significant respiratory depression, or in patients with certain cardiac conditions that predispose to QT prolongation. It is also contraindicated in patients taking monoamine‑oxidase inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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