Product image of Imovane (Zopiclone) supplied by GNH India

Imovane

Active Ingredient:
Zopiclone
Origin:
EU

Imovane (Zopiclone)

Zopiclone, the active ingredient in Imovane, is a cyclopyrrolone (non‑benzodiazepine hypnotic) presented as an oral tablet for oral use. It is prescribed to manage insomnia, helping adults who have difficulty initiating or maintaining sleep.

GNH India supplies Imovane as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for global healthcare providers.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

  • Zopiclone is a cyclopyrrolone hypnotic used to treat sleep disorders.
  • Insomnia: facilitates falling asleep and reduces nighttime awakenings.
  • Sleep onset insomnia: shortens the time required to fall asleep.
  • Sleep maintenance insomnia: helps maintain sleep throughout the night.

How It Works

  • Zopiclone acts as a positive allosteric modulator at the GABA‑A receptor complex. By binding to a distinct site, it enhances the receptor’s response to GABA, increasing chloride ion influx and strengthening inhibitory neurotransmission in the central nervous system, which produces a sedative‑hypnotic effect.

Side Effects

Common Side Effects

  • Drowsiness: feeling unusually sleepy during the day.
  • Dry mouth: reduced salivation leading to a dry sensation.
  • Headache: mild to moderate head pain.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Bitter or unpleasant taste.
  • Nausea: feeling of stomach upset.

Serious or Rare Side Effects

  • Complex sleep behaviours: sleepwalking, sleep‑driving, or other activities while not fully awake.
  • Allergic reactions: rash, itching, swelling, or difficulty breathing.
  • Mood changes: depression, anxiety, or suicidal thoughts.
  • Respiratory depression: slowed breathing, especially when combined with other depressants.
  • Dependence or withdrawal symptoms on abrupt discontinuation.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

  • Before prescribing Zopiclone, clinicians should consider several safety factors.
  • Assess renal function: adjust use in severe renal impairment.
  • Avoid alcohol: concurrent use may increase sedation and respiratory depression.
  • Limit duration: recommended for short‑term use only, typically up to 2–4 weeks.
  • Monitor for dependence: risk of tolerance and withdrawal with prolonged use.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit assessment.
  • Store at ambient temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Zopiclone may interact with other central nervous system depressants and drugs affecting its metabolism.

Major Interactions (Avoid)

  • Alcohol: additive CNS depression leading to excessive sedation.
  • Opioids: increased risk of respiratory depression and profound sedation.
  • Other CNS depressants (e.g., benzodiazepines, antihistamines): enhanced sedative effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may raise plasma concentrations of Zopiclone.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effectiveness.

Frequently Asked Questions

Imovane, whose active ingredient is Zopiclone, is prescribed to treat insomnia. It helps adults who have difficulty falling asleep, staying asleep, or experience frequent nighttime awakenings, providing a short‑term solution to improve sleep quality.

Zopiclone binds to a specific site on the GABA‑A receptor complex, acting as a positive allosteric modulator. This enhances the inhibitory effect of GABA, increasing chloride ion flow into neurons, which reduces neuronal excitability and produces a sedative‑hypnotic effect.

The dose of Imovane is individualized by the prescribing clinician based on the patient’s age, renal function, and overall health. Typical adult dosing ranges from 3.75 mg to 7.5 mg taken shortly before bedtime, but the exact regimen must be determined by a qualified healthcare professional.

Safety data for Zopiclone in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their healthcare provider.

To request Imovane, 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 and respond with pricing, availability, shipping details and any required import documentation.

The primary alternative to Zopiclone is the benzodiazepine class, such as temazepam. While both promote sleep, Zopiclone is a cyclopyrrolone with a slightly different receptor binding profile, often associated with a lower risk of next‑day sedation. However, both agents carry potential for dependence and should be used for short periods.

Imovane tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original blister pack or container, protect from moisture, heat and direct sunlight. Do not use the product if the packaging is damaged or the tablets appear discoloured.

Imovane is taken orally as a tablet with a glass of water. It should be taken shortly before bedtime, and patients should ensure they have a full night (7–8 hours) of sleep opportunity. The tablet should be swallowed whole and not crushed or chewed.

Serious risks include complex sleep behaviours such as sleepwalking or sleep‑driving, severe allergic reactions, respiratory depression (especially when combined with other depressants), and the potential for dependence or withdrawal symptoms after prolonged use. Patients should seek immediate medical attention if any of these occur.

Imovane is contraindicated in individuals with known hypersensitivity to Zopiclone or any excipients, severe hepatic or renal impairment, untreated severe sleep apnea, and in patients who are pregnant or breastfeeding unless the benefit outweighs the risk. Caution is also advised for those with a history of substance misuse.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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