Product image of Imipramine Crescent Pharma International (Imipramine Hydrochloride) supplied by GNH India

Imipramine Crescent Pharma International

Active Ingredient:
Imipramine Hydrochloride
Origin:
EU

Imipramine Crescent Pharma International (Imipramine Hydrochloride)

Imipramine, the active ingredient in Imipramine Crescent Pharma International, is a tricyclic antidepressant presented as an oral formulation for oral use. It is used to treat major depressive disorder, panic disorder and nocturnal enuresis in adults.

GNH India supplies Imipramine Crescent Pharma International as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Crescent Pharma International Limited

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Indications & Clinical Uses

  • Imipramine acts on monoamine neurotransmitter pathways and is indicated for several psychiatric and urological conditions.
  • Major depressive disorder: alleviates depressive symptoms and improves mood.
  • Panic disorder: reduces frequency and severity of panic attacks.
  • Nocturnal enuresis: decreases nighttime urinary leakage in children and adolescents.

How It Works

  • Imipramine inhibits the reuptake of norepinephrine and serotonin at neuronal synapses, thereby increasing their extracellular concentrations. The elevated monoamine levels enhance neurotransmission in central pathways that regulate mood, anxiety and bladder control, contributing to its therapeutic effects.

Side Effects

Imipramine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Dry mouth: reduced salivary flow.
  • Constipation: slowed gastrointestinal motility.
  • Drowsiness: sedation or fatigue.
  • Blurred vision: transient visual disturbances.
  • Weight gain: increased appetite or fluid retention.
  • Orthostatic hypotension: dizziness on standing.

Serious or Rare Side Effects

  • Cardiac arrhythmias: changes in heart rhythm.
  • Seizures: heightened risk in predisposed individuals.
  • Hepatotoxicity: liver enzyme elevations.
  • Severe hypotension: sudden drop in blood pressure.
  • Neuroleptic malignant syndrome-like reactions: high fever and muscle rigidity.
  • Suicide ideation: worsening depression in some patients.

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate patient history and monitor for specific risks.
  • Cardiovascular assessment: obtain baseline ECG in patients with heart disease.
  • Drug interactions: review concomitant medications for serotonergic activity.
  • Age considerations: use lower doses in elderly patients.
  • Renal/hepatic function: adjust dose if severe impairment is present.
  • Pregnancy and lactation: weigh benefits against potential risks.
  • Store at below 25°C: keep in original packaging, protect from moisture and light.

Avoid Interactions

Imipramine can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis.
  • SSRIs/SNRIs: potential serotonin syndrome.
  • Anticholinergic agents: additive dry mouth and constipation.
  • QT‑prolonging drugs: increased arrhythmia risk.
  • CYP2D6 inhibitors: elevated imipramine plasma levels.

Moderate Interactions (Monitor Closely):\n- Diuretics: may exacerbate orthostatic hypotension.

  • Antihypertensives: possible additive blood pressure lowering.
  • Alcohol: enhances CNS depression.
  • CNS depressants: increased sedation.
  • Anticonvulsants: may alter seizure threshold.

Frequently Asked Questions

Imipramine Crescent Pharma International is prescribed for major depressive disorder, panic disorder, and nocturnal enuresis. It belongs to the tricyclic antidepressant class and works by increasing levels of norepinephrine and serotonin in the brain, which helps improve mood, reduce anxiety attacks, and control nighttime urinary leakage.

Imipramine blocks the reuptake of the neurotransmitters norepinephrine and serotonin at neuronal synapses. By preventing their removal, the drug raises their concentration in the central nervous system, enhancing neurotransmission that regulates mood, anxiety, and bladder function, which underlies its therapeutic effects.

The appropriate dose of imipramine is determined by the prescribing healthcare professional based on the individual’s condition, age, weight, and response to therapy. Dosage adjustments may be needed over time, and patients should follow the prescriber’s instructions without self‑adjusting the amount.

Safety data for imipramine in pregnancy and lactation are limited. Healthcare providers must weigh the potential benefits against possible risks to the fetus or infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternative treatments or close monitoring with their clinician.

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.

Imipramine is a tricyclic antidepressant, differing from newer classes such as SSRIs and SNRIs in its mechanism and side‑effect profile. While effective for depression and anxiety, it often has more anticholinergic and cardiovascular effects, making it less commonly first‑line compared with newer agents that have more favorable tolerability.

Imipramine Crescent Pharma International should be stored at temperatures below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Imipramine is taken orally, usually in tablet form, with or without food as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include cardiac arrhythmias, especially in patients with pre‑existing heart disease, seizures, severe hypotension, hepatotoxicity, and the potential for worsening depression or suicidal thoughts, particularly at the start of therapy or when doses are changed.

Imipramine is contraindicated in patients with known hypersensitivity to the drug, recent myocardial infarction, uncontrolled narrow‑angle glaucoma, and those currently taking monoamine oxidase inhibitors. Caution is also advised for individuals with severe liver or kidney impairment, epilepsy, or a history of severe cardiac conduction disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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