Product image of Mucosolvan 1x Täglich (Ambroxol Hydrochloride) supplied by GNH India

Mucosolvan 1x Täglich

Active Ingredient:
Ambroxol Hydrochloride
Origin:
EU

Mucosolvan 1x Täglich (Ambroxol Hydrochloride)

Ambroxol Hydrochloride, the active ingredient in Mucosolvan 1x Täglich, is a mucolytic presented as an oral tablet for oral use. It facilitates the breakdown of thick bronchial mucus and is employed to improve clearance of secretions in patients with acute or chronic respiratory conditions such as bronchitis and COPD.

GNH India supplies Mucosolvan 1x Täglich as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product complies with EU quality standards, is manufactured under strict GMP conditions, and is available for bulk distribution.

Manufacturer / TM Owner

Opella Healthcare Austria Gmbh

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Indications & Clinical Uses

  • Ambroxol Hydrochloride acts as a mucolytic on the respiratory tract, helping to thin and mobilize mucus in several common pulmonary conditions.
  • Acute bronchitis: reduces mucus viscosity, facilitating expectoration and relieving cough.
  • Chronic bronchitis: improves mucus clearance, decreasing frequency of productive cough episodes.
  • COPD with productive cough: aids in thinning secretions, supporting airway patency and symptom control.
  • Upper respiratory tract infections with thick mucus: promotes drainage of nasal and bronchial secretions, easing congestion.

How It Works

  • Ambroxol Hydrochloride increases serous mucus production by stimulating bronchial epithelial cells, depolymerises mucopolysaccharide fibers to lower mucus viscosity, and enhances ciliary beat frequency, collectively accelerating the clearance of bronchial secretions.

Side Effects

Ambroxol Hydrochloride may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Taste alteration: a temporary bitter or metallic taste in the mouth.
  • Nausea: mild stomach upset after oral administration.
  • Diarrhea: loose stools occurring shortly after dosing.
  • Headache: mild to moderate head discomfort.
  • Dizziness: transient sensation of light‑headedness.

Serious or Rare Side Effects

  • Allergic reactions: rash, itching, swelling, or anaphylaxis in rare cases.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic enzyme elevation: abnormal liver function tests indicating possible liver involvement.

Precautions & Warnings

  • Before using Ambroxol Hydrochloride, consider the following precautions to ensure safe and effective therapy.
  • Pregnancy: consult a healthcare professional; safety data are limited.
  • Breastfeeding: caution advised as the drug may be excreted in breast milk.
  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Asthma: monitor for possible bronchospasm, especially in severe cases.
  • Drug interactions: review all concomitant medications with a pharmacist or physician.
  • Store at room temperature: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Ambroxol Hydrochloride can interact with certain medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Codeine‑containing antitussives: may counteract mucolytic effect.
  • MAO inhibitors: increased risk of adverse reactions.
  • Cytotoxic chemotherapy agents: potential enhancement of toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑2 agonists: additive bronchodilatory effect may require monitoring.
  • Antihistamines: may increase sedation or dry mouth.
  • Antacids: may alter absorption if taken simultaneously.

Frequently Asked Questions

Mucosolvan 1x Täglich is an over‑the‑counter mucolytic containing Ambroxol Hydrochloride, indicated to thin and loosen thick mucus in acute bronchitis, chronic bronchitis, COPD with productive cough, and upper respiratory tract infections, thereby facilitating expectoration.

Ambroxol stimulates serous cells in the bronchial epithelium to increase watery mucus production, depolymerises mucopolysaccharide fibers to lower viscosity, and enhances ciliary beat frequency, collectively promoting clearance of bronchial secretions.

The appropriate dose is determined by the prescribing healthcare professional based on the patient’s age, condition severity, and renal function. Patients should follow the label instructions and the prescriber’s guidance.

Safety data are limited; therefore, use during pregnancy should only occur if the potential benefit outweighs the risk and under medical supervision. Breastfeeding mothers should consult a clinician, as the drug may be secreted in milk.

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.

Compared with agents such as N‑acetylcysteine, Ambroxol has a dual action of stimulating serous mucus secretion and reducing viscosity, often resulting in faster symptom relief. Choice of therapy depends on clinical judgment, patient tolerance and local guidelines.

Keep the tablets at room temperature, below 25 °C, in the original blister pack. Protect them from moisture, direct sunlight and excessive heat to maintain stability.

The tablets are taken orally with a glass of water, preferably after meals to minimise gastrointestinal discomfort. Swallow whole; do not crush or chew unless directed by a healthcare professional.

Rare but serious adverse events include severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, and significant liver enzyme elevations. Patients should seek immediate medical attention if they experience rash, swelling, difficulty breathing, or jaundice.

Individuals with known hypersensitivity to Ambroxol or any excipients, patients with severe renal impairment without dose adjustment, and those taking contraindicated medications (e.g., certain MAO inhibitors) should avoid this product unless cleared by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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