Product image of Mucospas (Ambroxol Hydrochloride, Clenbuterol Hydrochloride) supplied by GNH India

Mucospas

Active Ingredient:
Ambroxol Hydrochloride, Clenbuterol Hydrochloride
Origin:
EU

Mucospas (Ambroxol Hydrochloride, Clenbuterol Hydrochloride)

Ambroxol Hydrochloride and Clenbuterol Hydrochloride, the active ingredients in Mucospas, are mucolytic and β2‑adrenergic agonist drugs presented as an oral formulation for oral use. They are used to relieve mucus congestion and bronchospasm in patients with acute or chronic respiratory conditions.

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

Manufacturer / TM Owner

Opella Healthcare Austria Gmbh

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Indications & Clinical Uses

  • Mucospas, containing a mucolytic and a β2‑adrenergic agonist, is indicated for disorders of the respiratory tract that involve mucus hypersecretion or bronchoconstriction.
  • Acute bronchitis: reduces mucus viscosity and improves cough clearance.
  • Chronic bronchitis (COPD): helps clear sputum and eases breathing.
  • Asthma exacerbations: provides bronchodilation to relieve bronchospasm.
  • Bronchospasm associated with respiratory infections: relaxes airway smooth muscle and facilitates mucus clearance.

How It Works

  • Ambroxol stimulates surfactant production by type II pneumocytes and enhances ciliary activity, lowering mucus viscosity and promoting clearance. Clenbuterol selectively activates β2‑adrenergic receptors on bronchial smooth muscle, increasing intracellular cyclic AMP, which leads to muscle relaxation and bronchodilation. The combined actions improve airway patency and reduce cough in obstructive respiratory diseases.

Side Effects

Common Side Effects

  • Nausea: mild gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Tremor: fine muscle shaking, especially in the hands.
  • Palpitations: awareness of heartbeat acceleration.
  • Dry mouth: reduced salivation.
  • Dizziness: light‑headed sensation.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm requiring medical attention.
  • Severe bronchospasm: paradoxical worsening of airway constriction.
  • Hypokalemia: low blood potassium levels, may cause muscle weakness.
  • Anaphylaxis: acute allergic reaction with rash, swelling, and airway compromise.
  • Tachycardia: sustained rapid heart rate.
  • Hypertension: elevated blood pressure beyond normal range.

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for adverse reactions.
  • Assess renal and hepatic function: adjust use if organ impairment is present.
  • Monitor cardiac status: avoid in uncontrolled heart disease.
  • Use caution in hyperthyroidism: β2‑agonists may exacerbate symptoms.
  • Avoid in uncontrolled hypertension: risk of further blood pressure rise.
  • Check for known hypersensitivity to either component.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Mucospas may interact with other medicines that affect cardiovascular or electrolyte balance.

Major Interactions (Avoid)

  • Beta‑blockers: antagonize bronchodilator effect.
  • MAO inhibitors: increase risk of hypertensive crisis.
  • Potassium‑wasting diuretics: may precipitate hypokalemia.
  • Other sympathomimetics: additive cardiovascular stimulation.

Moderate Interactions (Monitor Closely)

  • Anticholinergics: may enhance anticholinergic side effects.
  • Theophylline: increased risk of tachyarrhythmia.
  • ACE inhibitors: potential for additive hypotensive effect.
  • NSAIDs: may blunt bronchodilator response.

Frequently Asked Questions

Mucospas is prescribed for respiratory tract disorders that involve excess mucus or bronchoconstriction, such as acute or chronic bronchitis, chronic obstructive pulmonary disease (COPD), asthma exacerbations, and bronchospasm linked to respiratory infections.

Ambroxol stimulates surfactant secretion by type II pneumocytes and enhances ciliary activity, which lowers mucus viscosity and promotes clearance of secretions from the airways, helping to ease productive cough.

The specific dose and dosing schedule of Mucospas are determined by the prescribing clinician based on the patient’s age, severity of disease, and renal or hepatic function. Patients should follow the prescriber’s instructions exactly.

Safety data for Mucospas in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and consider alternative therapies when appropriate. Women should discuss use with their obstetrician before starting treatment.

To request Mucospas, 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 required import documentation.

Mucospas combines Ambroxol, a well‑established mucolytic, with Clenbuterol, a selective β2‑agonist. Compared with single‑agent products, this dual action can simultaneously reduce mucus thickness and relax airway smooth muscle, potentially offering broader symptom relief in mixed obstructive conditions.

Mucospas should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and heat sources to maintain stability.

Mucospas is taken orally, typically as a tablet or capsule, with water. The exact administration instructions, such as taking with or without food, are provided by the prescribing clinician.

Serious risks include cardiac arrhythmias, severe bronchospasm, hypokalemia, hypertension, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience palpitations, chest pain, sudden worsening of breathing, or signs of an allergic response.

Mucospas is contraindicated in individuals with known hypersensitivity to Ambroxol, Clenbuterol, or any excipients, as well as patients with uncontrolled hypertension, significant cardiac arrhythmias, or severe hyperthyroidism. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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