


Ask a doctor about a prescription for MONTELUKAST TARBIS FARMA 10 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Montelukast Tarbis Farma 10 mg Film-Coated Tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
What is Montelukast Tarbis Farma
Montelukast is a leukotriene receptor antagonist that blocks substances called leukotrienes.
How Montelukast works
Leukotrienes cause the airways to narrow and swell, and can cause symptoms of asthma and allergic rhinitis. By blocking the leukotrienes, Montelukast improves asthma symptoms, helps control asthma, and improves symptoms of seasonal allergic rhinitis (also known as hay fever or seasonal allergic rhinitis).
When to use Montelukast
Your doctor has prescribed Montelukast to treat asthma and prevent asthma symptoms during the day and night.
Depending on your symptoms and the severity of your asthma, your doctor will determine how you should use Montelukast.
What is asthma?
Asthma is a chronic disease.
Asthma includes:
The symptoms of asthma include: Cough, wheezing, and chest congestion.
What are seasonal allergies?
Seasonal allergies (also known as hay fever or seasonal allergic rhinitis) are an allergic reaction often caused by airborne pollen from trees, grass, and weeds. The symptoms of seasonal allergies typically include: stuffy nose, runny nose; sneezing; itchy, watery, swollen, red, and sore eyes.
Tell your doctor about any allergy or medical problem you have now or have had.
Do not take Montelukast Tarbis Farma
Warnings and precautions
Consult your doctor or pharmacist before starting this medication.
Various neuropsychiatric events (such as changes related to behavior and mood, depression, and suicidal tendencies) have been reported in patients of all ages treated with montelukast (see section 4). If you develop such symptoms while taking montelukast, you should communicate with your doctor.
Children and adolescents
Do not give this medicine to children under 15 years of age.
For pediatric patients under 18 years of age, other formulations of this medicine are available based on the age range.
Other medicines and Montelukast Tarbis Farma
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including those obtained without a prescription.
Some medicines may affect the way montelukast works, or montelukast may affect the way other medicines work.
Before taking this medicine, tell your doctor if you are taking the following medicines:
Montelukast Tarbis Farma with food and drinks
This medicine can be taken with or without food.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
Your doctor will assess whether you can take montelukast during this period.
Breastfeeding
It is not known whether montelukast appears in breast milk. If you are breastfeeding or plan to breastfeed, you should consult your doctor before taking montelukast.
Driving and using machines
Montelukast is not expected to affect your ability to drive a car or operate machinery. However, individual responses to the medication may vary. Certain side effects (such as dizziness and drowsiness) that have been reported with montelukast may affect the patient's ability to drive or operate machinery.
Montelukast Tarbis Farma contains lactose
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Montelukast Tarbis Farma contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is, essentially “sodium-free”.
Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
For adults and adolescents 15 years of age and older:
The recommended dose is one 10 mg tablet daily in the evening. If you are taking this medicine, make sure you do not take any other product that contains the same active ingredient, montelukast.
This medicine is taken orally.
Montelukast 10 mg can be taken with or without food.
If you take more Montelukast Tarbis Farma than you should
Seek immediate medical attention.
In most cases of overdose, no adverse effects were reported. The symptoms that occurred most frequently reported in overdose in adults and children were abdominal pain, drowsiness, thirst, headache, vomiting, and hyperactivity.
In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take this medicine
Try to take this medicine as prescribed. However, if you miss a dose, just resume your usual schedule of one tablet once a day.
Do not take a double dose to make up for missed doses.
If you stop taking Montelukast Tarbis Farma
This medicine may only treat your asthma if you continue to take it. It is important that you continue to take this medicine for as long as your doctor prescribes it. It will help control your asthma.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
In clinical trials conducted with montelukast 10 mg film-coated tablets, the adverse effects related to the administration of the medicine and most frequently reported (may affect up to 1 in 10 people), were:
These adverse effects were generally mild and occurred with a higher frequency in patients treated with montelukast than with placebo (a pill that does not contain medicine).
Serious side effects
Consult your doctor immediatelyif you observe any of the following side effects, which may be serious and may require urgent medical treatment.
Uncommon (may affect up to 1 in 100 people):
Rare (may affect up to 1 in 1,000 people):
Very rare (may affect up to 1 in 10,000 people):
Other side effects reported during the marketing of the medicine
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Uncommon (may affect up to 1 in 100 people):
Rare (may affect up to 1 in 1,000 people):
Very rare (may affect up to 1 in 10,000 people):
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if they are not listed in this leaflet. You can also report side effects directly via the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es.
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the blister after CAD. The first two numbers indicate the month; the last four numbers indicate the year. The expiry date is the last day of the month that is indicated.
This medicine does not require any special storage temperature.
Store in the original packaging to protect from moisture.
Medicines should not be disposed of via wastewater or household waste. Place the packaging and any unused medicine in the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
Composition of Montelukast Tarbis Farma
The active substance is montelukast.
Each tablet contains montelukast sodium equivalent to 10 mg of montelukast.
The other ingredients are:
Core of the tablet: lactose monohydrate, mannitol (E421), sodium croscarmellose, hypromellose (E 463), microcrystalline cellulose (PH 112), magnesium stearate.
Coating: hypromellose 6cP (E464), titanium dioxide (E 171), hypromellose (E 463), carnauba wax, yellow iron oxide (E 172), red iron oxide (E 172).
Appearance of the product and contents of the pack
Film-coated tablet.
Beige, square-shaped tablet with rounded edges (7.9 x 7.9 mm), film-coated tablets, marked 'I' on one face and '114' on the other.
Blister packs: 28, 30, 90, 98, and 100 tablets.
Not all pack sizes may be marketed.
Marketing authorization holder
Tarbis Farma S.L.
Gran Vía Carlos III, 94
08028 Barcelona
Spain
Manufacturer
Pharmadox Healthcare Ltd.
KW20A Kordin Industrial Park
Paola, PLA 3000
Malta
Amarox Pharma B.V.
Rouboslaan 32
Voorschooten, 2252TR
Netherlands
This medicine is authorized in the Member States of the European Economic Area under the following names:
Netherlands: Montelukast Amarox 10 mg, filmomhulde tabletten
Spain: Montelukast Tarbis Farma 10 mg comprimidos recubiertos con película EFG
Sweden: Montelukast Amarox 10 mg filmdragerade tabletter
Date of last revision of this leaflet: December 2023
Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es
The average price of MONTELUKAST TARBIS FARMA 10 mg FILM-COATED TABLETS in November, 2025 is around 21.06 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for MONTELUKAST TARBIS FARMA 10 mg FILM-COATED TABLETS – subject to medical assessment and local rules.