Escitalopram Sandoz: detailed information

Package leaflet: Information for the patient

Escitalopram Sandoz 5 mg film-coated tablets, 10 mg film-coated tablets, 15 mg film-coated tablets, 20 mg film-coated tablets

Generic medicine
Please read all of this leaflet carefully before taking this medicine because it contains
important information for you.

Keep this leaflet. You may need to read it again.
If you have any questions, ask your doctor or pharmacist.
This medicine has been prescribed for you only. Do not give it to other people, even if they have the same symptoms as yours, as it may be harmful.
If you experience any side effect, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.

Contents of this leaflet:

What Escitalopram Sandoz is and what it is used for
What you need to know before taking Escitalopram Sandoz
How to take Escitalopram Sandoz
Possible side effects
How to store Escitalopram Sandoz
Contents of the pack and other information

1. What Escitalopram Sandoz is and what it is used for

Escitalopram Sandoz contains the active substance escitalopram. Escitalopram Sandoz belongs to a
group of antidepressants called selective serotonin reuptake inhibitors (SSRIs). These
medicines work on the serotonin system in the brain by increasing the level of serotonin.
Disturbances in the serotonin system are considered an important factor in the development of
depression and related disorders.
Escitalopram Sandoz is used to treat depression (major depressive episodes) and anxiety
disorders (such as panic disorder with or without agoraphobia, social anxiety disorder, generalized anxiety disorder, and obsessive-compulsive disorder).
It may take a couple of weeks before you start to feel better. Continue taking Escitalopram Sandoz even if it takes some time before you notice an improvement in your condition.
You should contact your doctor if you do not feel better or if you feel worse.

2. What you should know before taking Escitalopram Sandoz

Do not take Escitalopram Sandoz

if you are allergic to escitalopram or to any of the other ingredients of this medicine (listed in section 6).
if you are taking other medicines belonging to a group called "MAO inhibitors", including selegiline (used in the treatment of Parkinson's disease), moclobemide (used in the treatment of depression), or linezolid (an antibiotic).
if you have been born with or have experienced an episode of heart rhythm disorder (identified by an ECG; a test performed to assess heart function).
if you are taking medicines for heart rhythm problems or that may affect heart rhythm (see also section 2 “Other medicines and Escitalopram Sandoz”).

Warnings and precautions
Talk to your doctor or pharmacist before taking Escitalopram Sandoz.
Inform your doctor if you have any other disorder or illness, as this may need to be taken into account by your doctor. In particular, inform your doctor if:

you suffer from epilepsy. Treatment with Escitalopram Sandoz should be discontinued if seizures occur for the first time or if there is an increase in seizure frequency (see also section 4 “Possible side effects”).
you have hepatic or renal impairment. Your doctor may need to adjust your dose.
you have diabetes. Treatment with Escitalopram Sandoz may alter blood sugar levels. You may need to adjust your insulin dose and/or your oral blood sugar-lowering medication.
you have low sodium levels in the blood.
you have a tendency to develop bleeding or bruising easily, or if you are pregnant (see section “Pregnancy”).
you have a tendency to develop bleeding or bruising easily.
you are undergoing electroconvulsive therapy.
you have coronary heart disease.
you suffer or have suffered from heart problems or have recently had a heart attack.
you have a low resting heart rate and/or if you know you have electrolyte imbalances due to severe and prolonged diarrhoea or vomiting (feeling unwell) or if you are using diuretics (medicines to increase urine production).
upon standing up, you experience a rapid or irregular heartbeat, fainting, collapse, or dizziness, which could indicate an abnormality in heart rhythm function.
you have or have previously had eye problems, such as certain types of glaucoma (increased pressure in the eye).

Please note
Some patients with bipolar disorder may enter a manic phase. This is characterized by unusual and rapidly changing thoughts, inappropriate happiness, and excessive physical activity.
If you experience these symptoms, consult your doctor.
Symptoms such as agitation or difficulty sitting or standing still may occur during the first weeks of treatment. Inform your doctor immediately if these symptoms occur.
Medicines such as Escitalopram Sandoz (so-called selective serotonin reuptake inhibitors (SSRIs) and serotonin-noradrenaline reuptake inhibitors (SNRIs)) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have been observed to persist after discontinuation of treatment.
Suicidal thoughts and worsening of depression or anxiety disorder
If you are depressed and/or suffer from anxiety disorders, you may sometimes have thoughts of self-harm or suicidal thoughts. These may increase when you first start taking antidepressants, as these medicines take time to work, usually about two weeks, but sometimes longer.
You may be more likely to have these types of thoughts:

If you have previously had suicidal or self-harming thoughts.
If you are a young adult. Data from clinical trials have shown an increased risk of suicidal behaviour in adults under 25 years of age with psychiatric disorders who were treated with an antidepressant. If at any time you have thoughts of self-harm or suicide, contact your doctor or go immediately to hospital.

It may be helpful to tell a relative or close friend that you suffer from depression or an anxiety disorder, and ask them to read this leaflet. You may ask them to inform you if they believe your depression or anxiety is worsening, or if they are concerned about any changes in your behaviour.
Children and adolescents
Escitalopram Sandoz is normally not to be used in children and adolescents under 18 years of age. In addition, you should know that patients under 18 years of age have an increased risk of side effects such as suicide attempts, suicidal thoughts, and hostility (mainly aggression, oppositional behaviour, and anger) when taking this class of medicines.
Nevertheless, your doctor may prescribe Escitalopram Sandoz to patients under 18 years of age if they consider it the best option for them. If your doctor has prescribed Escitalopram Sandoz to a patient under 18 years of age and you wish to obtain further information, please consult your doctor again. You must inform your doctor if any of the symptoms described above appear or worsen in patients under 18 years of age taking Escitalopram Sandoz. In addition, the long-term safety effects of Escitalopram Sandoz on growth, maturation, and cognitive and behavioural development in this age group have not yet been established.
Other medicines and Escitalopram Sandoz
Inform your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Inform your doctor if you are taking any of the following medicines:

Non-selective monoamine oxidase inhibitors (MAOIs) containing phenelzine, iproniazid, isocarboxazid, nialamide, or tranylcypromine as active ingredients. If you have taken any of these medicines, you must wait 14 days before starting Escitalopram Sandoz. After stopping Escitalopram Sandoz, you must wait 7 days before taking any of these medicines.
Reversible selective MAO-A inhibitors, containing moclobemide (used to treat depression).
Irreversible MAO-B inhibitors, containing selegiline (used to treat Parkinson's disease). These increase the risk of side effects.
The antibiotic linezolid.
Lithium (used in the treatment of bipolar disorder) and tryptophan.
Imipramine and desipramine (both used to treat depression).
Sumatriptan and similar medicines (used to treat migraine) and tramadol (used for severe pain). These increase the risk of side effects.
Cimetidine, lansoprazole, and omeprazole (used to treat stomach ulcers), fluconazole (used to treat fungal infections), fluvoxamine (an antidepressant), and ticlopidine (used to reduce the risk of stroke). These medicines may cause an increase in blood levels of escitalopram.
St. John's wort ( Hypericum perforatum ) – a herbal remedy used for depression.
Acetylsalicylic acid and non-steroidal anti-inflammatory drugs (NSAIDs) (medicines used to relieve pain or to thin the blood, so-called anticoagulants). These may increase the tendency to bleed.
Warfarin, dipyridamole, and phenprocoumon (medicines used to thin the blood, so-called anticoagulants). Your doctor will likely monitor your blood clotting time when starting and stopping Escitalopram Sandoz to ensure that your anticoagulant dose remains appropriate.
Mefloquine (used to treat malaria), bupropion (used to treat depression), and tramadol (used to treat severe pain) due to a possible risk of lowering the seizure threshold.
Neuroleptics (medicines to treat schizophrenia, psychosis) and antidepressants (tricyclic antidepressants and SSRIs) are associated with a possible risk of lowering the seizure threshold.
Flecainide, propafenone, and metoprolol (used in cardiovascular diseases), clomipramine and nortriptyline (antidepressants), and risperidone, thioridazine, and haloperidol (antipsychotics). Dose adjustment of Escitalopram Sandoz may be necessary.
Medicines that decrease plasma levels of potassium or magnesium, as these conditions increase the risk of life-threatening heart rhythm disturbances.

Do not take Escitalopram Sandoz if you are taking medicines for heart rhythm problems or that may affect heart rhythm, such as, for example, class IA and III antiarrhythmics, antipsychotics (such as phenothiazine derivatives, pimozide, haloperidol), tricyclic antidepressants, certain antimicrobial agents (such as sparfloxacin, moxifloxacin, intravenous erythromycin, pentamidine, antimalarial treatments, particularly halofantrine), or certain antihistamines (astemizole, hydroxyzine, mizolastine). If you have any further doubts, contact your doctor.
Escitalopram Sandoz with food, drinks and alcohol
Escitalopram Sandoz may be taken with or without food (see section 3 “How to take Escitalopram Sandoz”).
As with many medicines, it is not recommended to combine Escitalopram Sandoz with alcohol, although interactions with alcohol are not expected.
Pregnancy, breastfeeding and fertility
If you are pregnant, think you may be pregnant, are planning to become pregnant, or are breastfeeding, consult your doctor or pharmacist before taking this medicine. Do not take Escitalopram Sandoz if you are pregnant or breastfeeding, unless you and your doctor have discussed the risks and benefits.
If you take Escitalopram Sandoz during the last 3 months of pregnancy, you should know that the newborn may experience the following symptoms: breathing difficulties, bluish skin colour, seizures, changes in body temperature, feeding difficulties, vomiting, low blood sugar levels, muscle stiffness or floppiness, hyperactive reflexes, tremors, restlessness, irritability, lethargy, continuous crying, drowsiness, and sleep disturbances. If your newborn shows any of these symptoms, contact your doctor immediately.
Ensure that your midwife and/or doctor know that you are being treated with Escitalopram Sandoz. Medicines such as Escitalopram Sandoz, if taken during pregnancy, particularly during the last 3 months of pregnancy, may increase the risk of a serious condition in newborns called persistent pulmonary hypertension of the newborn (PPHN), which causes the baby to breathe faster and develop a bluish skin colour. These symptoms usually occur within the first 24 hours after birth. Contact your midwife and/or doctor immediately if your baby shows these symptoms.
If Escitalopram Sandoz is used during pregnancy, it must never be stopped abruptly.
If you take Escitalopram Sandoz near the end of pregnancy, there may be an increased risk of heavy vaginal bleeding shortly after delivery, especially if you suffer from bleeding disorders (tendency to bleed). Inform your doctor or midwife that you are taking Escitalopram Sandoz, so they can advise you on what to do.
Escitalopram is expected to be excreted in breast milk.
Citalopram, a medicine similar to escitalopram, has shown in animal studies to reduce sperm quality. In theory, this could affect fertility, but the impact on human fertility has not yet been observed.
Driving and using machines
Do not drive or operate machinery until you know how Escitalopram Sandoz affects you.
Escitalopram Sandoz contains lactose and sodium
If your doctor has diagnosed you with an intolerance to certain sugars, contact them before taking this medicine.
This medicine contains less than 1 mmol (23 mg) of sodium per film-coated tablet, i.e., essentially “sodium-free”.

3. How to take Escitalopram Sandoz

Take this medicine exactly as prescribed by your doctor. If you are unsure, consult your doctor or pharmacist.

Adults
Depression:
The usual recommended dose is 10 mg taken once daily. Your doctor may increase the dose up to a maximum of 20 mg per day.

Panic disorder:
The initial dose is 5 mg taken once daily for the first week, before increasing the dose to 10 mg per day. The dose may be further increased by your doctor up to a maximum of 20 mg per day.

Social anxiety disorder/social phobia:
The usual recommended dose is 10 mg taken as a single daily dose. Your doctor may reduce the dose to 5 mg per day or increase it up to a maximum of 20 mg per day, depending on your response to the medicine.

Generalised anxiety disorder:
The usual recommended dose is 10 mg taken as a single daily dose. The dose may be increased by your doctor up to a maximum of 20 mg per day.

Obsessive-compulsive disorder:
The usual recommended dose is 10 mg taken as a single daily dose. The dose may be increased by your doctor up to a maximum of 20 mg per day.

Elderly (over 65 years of age)
The recommended initial dose of Escitalopram Sandoz is 5 mg as a single daily dose. Your doctor may increase the dose up to 10 mg per day.

Use in children and adolescents (under 18 years of age)
Escitalopram Sandoz should normally not be given to children and adolescents (for further information, see section 2 “Warnings and precautions”).

Reduced kidney function
Caution is advised in patients with severely reduced renal function. Take as prescribed by your doctor.

Reduced liver function
Patients with liver problems should not receive more than 10 mg per day. Take as prescribed by your doctor.

Patients known to be poor metabolisers of the enzyme CYP2C19
Patients with this known genotype should not receive more than 10 mg per day. Take as prescribed by your doctor.

Method of administration
You may take Escitalopram Sandoz with or without food. Swallow the tablet with some water.
Only for Escitalopram Sandoz 10 mg: if necessary, you may divide the tablet into two equal parts.
Only for Escitalopram Sandoz 15 mg: if necessary, you may divide the tablet into three equal parts.
Only for Escitalopram Sandoz 20 mg: if necessary, you may divide the tablet into four equal parts.

Duration of treatment

It may take a few weeks before you start to feel better. Therefore, you should continue taking Escitalopram Sandoz, even if it takes time before you notice an improvement in your condition.
Do not change the dose of the medicine without first discussing it with your doctor.
Continue taking Escitalopram Sandoz for as long as your doctor prescribes it. If you stop treatment too early, your symptoms may return. It is recommended to continue treatment for at least 6 months after you start feeling well again.

If you take more Escitalopram Sandoz than you should
If you have taken an excessive amount of Escitalopram Sandoz, contact your doctor or the nearest hospital emergency department immediately. Do this even if you do not have any signs of discomfort. Some symptoms of overdose may include: dizziness, tremors, agitation, seizures, coma, nausea, vomiting, changes in heart rhythm, decreased blood pressure, and disturbances in fluid/electrolyte balance. Take the box/packaging of Escitalopram Sandoz with you when you go to the doctor or hospital.

If you forget to take Escitalopram Sandoz
Do not take a double dose to make up for the missed dose. If you forget to take a dose and remember before going to bed, take it immediately and continue as usual the next day. If you remember only during the night or the following day, skip the missed dose and take the next dose at the usual time.

If you stop taking Escitalopram Sandoz
Do not stop taking Escitalopram Sandoz unless your doctor tells you to. After completing the treatment course, it is generally advisable to gradually reduce the dose of Escitalopram Sandoz over several weeks.

When stopping treatment with Escitalopram Sandoz, especially if stopped abruptly, withdrawal symptoms may occur. These are common when treatment with Escitalopram Sandoz is discontinued. The risk is greater when Escitalopram Sandoz has been used for a long time, at high doses, or when the dose is reduced too quickly. Most people find that these symptoms are mild and resolve on their own within 2 weeks. However, in some patients, withdrawal symptoms may be severe or prolonged (2–3 months or longer). If you experience severe withdrawal symptoms when stopping treatment with Escitalopram Sandoz, contact your doctor. The doctor may advise you to restart taking your tablets and reduce the dose more slowly.

Withdrawal symptoms include: dizziness (unsteadiness or loss of balance), prickling or pinprick sensations, burning sensations (less frequent), electric shock-like sensations, even in the head, sleep disturbances (vivid dreams, nightmares, difficulty sleeping), feeling anxious, headache, feeling unwell (nausea), sweating (including night sweats), feeling restless or agitated, tremor (shaking), feeling confused or disoriented, emotional instability or irritability, diarrhoea (loose stools), visual disturbances, fluctuating or pounding heartbeat (palpitations).

Escitalopram Sandoz 15 mg film-coated tablets:
the tablet can be divided into three doses. Consult your doctor if you think you may not be able to divide the tablet correctly. Your doctor will prescribe a tablet of a lower strength.

If you have any doubts about how to use this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
Side effects are usually mild and normally disappear after a few weeks of treatment. Keep in mind that many of the effects listed may also be symptoms of your illness and will therefore improve as you start to feel better.
If you experience any of the following symptoms, consult your doctor or go to hospital immediately:
Uncommon (may affect up to 1 in 100 people)

Unusual bleeding, including gastrointestinal bleeding

Rare (may affect up to 1 in 1,000 people)

Swelling of the skin, tongue, lips, throat or face, hives or difficulty breathing or swallowing (severe allergic reaction)
High fever, agitation, confusion, tremors and sudden muscle contractions, which may be signs of a rare condition known as serotonin syndrome

Not known (frequency cannot be estimated from the available data)

Difficulty urinating
Seizures (fits), see also section 2 “Warnings and precautions”
Yellowing of the skin and whites of the eyes, which are signs of impaired liver function/hepatitis
Rapid or irregular heartbeat, feeling faint, which may be symptoms of a life-threatening condition known as Torsade de Pointes
Self-harming or suicidal thoughts, see also section “Warnings and precautions”
Sudden swelling of the skin or mucous membranes (angioedema)

In addition to those listed above, the following side effects have been reported:
Very common (may affect more than 1 in 10 people)

Feeling unwell (nausea)
Headache

Common (may affect up to 1 in 10 people)

Stuffy or runny nose (sinusitis)
Decreased or increased appetite
Anxiety, restlessness, abnormal dreams, difficulty falling asleep, drowsiness, dizziness, yawning, tremors, tingling sensations on the skin
Diarrhoea, constipation, vomiting, dry mouth
Increased sweating
Muscle and joint pain (arthralgia and myalgia)
Sexual disorders (delayed ejaculation, erection problems, reduced sexual drive, women may have difficulty achieving orgasm)
Fatigue, fever
Weight gain

Uncommon (may affect up to 1 in 100 people)

Hives, skin rash, itching
Teeth grinding, restlessness, nervousness, panic attacks, confusion
Changes in taste, sleep disorders, fainting (syncope)
Dilated pupils (mydriasis), visual disturbances, ringing in the ears (tinnitus)
Hair loss
Excessive menstrual bleeding
Irregular menstrual periods
Decrease in body weight
Fast heartbeat
Swelling of arms or legs
Nosebleeds

Rare (may affect up to 1 in 1,000 people)

Aggression, depersonalisation, hallucinations
Slowed heartbeat

Not known (frequency cannot be estimated from the available data):

Decreased sodium levels in the blood (symptoms include nausea and malaise with muscle weakness or confusion)
Dizziness upon standing due to low blood pressure (orthostatic hypotension)
Abnormal liver function tests (increased levels of liver enzymes in the blood)
Movement disorders (involuntary muscle movements)
Painful erections (priapism)
Signs of abnormal bleeding, for example bleeding of the skin and mucous membranes (bruising) and low platelet count in the blood (thrombocytopenia)
Increased secretion of a hormone called ADH, causing water retention and reduced blood sodium levels (inappropriate ADH secretion)
Increased blood levels of the hormone prolactin
Milk production in men and women who are not breastfeeding
Mania
An increased risk of bone fractures has been observed in patients taking this type of medicine
Changes in heart rhythm (called “prolongation of the QT interval”, assessed by an ECG which records the electrical activity of the heart)
Heavy vaginal bleeding shortly after childbirth (postpartum haemorrhage), see section 2, Pregnancy, for further information.

In addition, some side effects are known to occur with medicines that act similarly to escitalopram (the active substance in Escitalopram Sandoz). These include:

Motor restlessness (akathisia)
Loss of appetite

Reporting of side effects
If you get any side effects, including ones not listed in this leaflet, talk to your doctor or pharmacist.
You can also report side effects directly via the national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse
By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store Escitalopram Sandoz

Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the label or packaging after "Exp.". The expiry date refers to the last day of that month.
This medicine does not require any special storage conditions.
HDPE bottle
After first opening, the tablets can be stored in the opened HDPE bottle for a maximum period of 6 months. Do not store the opened bottle at a temperature above 25°C.
After this 6-month period, any remaining tablets in the opened HDPE bottle must not be used and should be disposed of.
Do not dispose of any medicine via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. This will help protect the environment.

6. Package Contents and Other Information

What Escitalopram Sandoz Contains

The active substance is escitalopram. Each film-coated tablet contains 5 mg/10 mg/15 mg/20 mg of the active substance escitalopram (as oxalate).
The excipients are:
Tablet core: Lactose monohydrate, microcrystalline cellulose, sodium croscarmellose, hypromellose, magnesium stearate, anhydrous colloidal silica.
Tablet coating: Hypromellose, Macrogol 6000, Titanium dioxide (E 171), Talc.

Description of the Appearance of Escitalopram Sandoz and Contents of the Package
Escitalopram Sandoz 5 mg: The tablets are white, round, film-coated, with a diameter of 5.7–6.3 mm.

Escitalopram Sandoz 10 mg:
The tablets are white, oval, film-coated, with a score line on one side, with a length of 7.7–8.3 mm and a thickness of 5.2–5.8 mm.

Escitalopram Sandoz 15 mg:
The tablets are white, oval, film-coated, with two score lines on both sides, with a length of 12.7–13.3 mm and a thickness of 4.7–5.3 mm.

Escitalopram Sandoz 20 mg:
The tablets are white, round, film-coated, with a cross-score on both sides, with a diameter of 9.2–9.8 mm.

Escitalopram Sandoz is available in the following pack sizes:
Blister packs in OPA-Al-PVC/Al in cardboard boxes:
7, 10, 14, 20, 28, 30, 50, 56, 56x1, 60, 60x1, 90, 98, 98x1, 100, 100x1, 200 and 500 film-coated tablets.

HDPE bottles with PP screw cap and desiccant:
28, 30, 56, 60, 98, 100 and 250 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer
Sandoz S.p.A.
Viale Luigi Sturzo 43
20154 Milan
Italy

Manufacturers
Lek Pharmaceuticals d.d., Verovškova 57, 1526 Ljubljana, Slovenia
LEK S.A., ul. Domaniewska 50 C, 02-672 Warszawa, Poland
Salutas Pharma GmbH, Otto-von-Guericke-Allee 1, 39179 Barleben, Germany
LEK S.A., ul. Podlipie 16, 95-010 Stryków, Poland
Lek Pharmaceuticals d.d., Trimlini 2D, 9220 Lendava

This medicinal product is authorized in the European Economic Area Member States under the following names:
Austria: Etalsapam 5 mg – Filmtabletten
Etalsapam 10 mg – Filmtabletten
Etalsapam 15 mg – Filmtabletten
Etalsapam 20 mg – Filmtabletten

Belgium: Escitalopram Sandoz 5 mg – filmomhulde tabletten
Escitalopram Sandoz 10 mg – filmomhulde tabletten
Escitalopram Sandoz 15 mg – filmomhulde tabletten
Escitalopram Sandoz 20 mg – filmomhulde tabletten

Bulgaria: Escitalon

Czech Republic: Escirdec Neo 10 mg
Escirdec Neo 20 mg

Denmark: Escitalopram Sandoz

Estonia: Ciraset 10 mg
Ciraset 20 mg

Greece: Escitalopram/Sandoz

Spain: Escitalopram Sandoz 10 mg comprimidos recubiertos con película EFG
Escitalopram Sandoz 15 mg comprimidos recubiertos con película EFG
Escitalopram Sandoz 20 mg comprimidos recubiertos con película EFG

France: Escitalopram Sandoz 5 mg, comprimé pelliculé
Escitalopram Sandoz 10 mg, comprimé pelliculé sécable
Escitalopram Sandoz 15 mg, comprimé pelliculé sécable
Escitalopram Sandoz 20 mg, comprimé pelliculé sécable

Finland: Escitalopram Sandoz 5 mg tabletti, kalvopäällysteinen
Escitalopram Sandoz 10 mg tabletti, kalvopäällysteinen
Escitalopram Sandoz 15 mg tabletti, kalvopäällysteinen
Escitalopram Sandoz 20 mg tabletti, kalvopäällysteinen

Hungary: Escitalopram Sandoz 5 mg filmtabletta
Escitalopram Sandoz 10 mg filmtabletta
Escitalopram Sandoz 15 mg filmtabletta
Escitalopram Sandoz 20 mg filmtabletta

Italy: ESCITALOPRAM SANDOZ

Luxembourg: Escitalopram Sandoz 5 mg – comprimés pelliculés
Escitalopram Sandoz 10 mg – comprimés pelliculés
Escitalopram Sandoz 15 mg – comprimés pelliculés
Escitalopram Sandoz 20 mg – comprimés pelliculés

Netherlands: Escitalopram Sandoz 5 mg, filmomhulde tabletten
Escitalopram Sandoz 10 mg, filmomhulde tabletten
Escitalopram Sandoz 15 mg, filmomhulde tabletten
Escitalopram Sandoz 20 mg, filmomhulde tabletten

Norway: Escitalopram Sandoz

Poland: Pramatis

Portugal: Escitalopram Sandoz

Romania: Escitalopram Sandoz 5 mg comprimate filmate
Escitalopram Sandoz 10 mg comprimate filmate
Escitalopram Sandoz 15 mg comprimate filmate
Escitalopram Sandoz 20 mg comprimate filmate

Slovenia: Citafort 5 mg filmsko obložene tablete
Citafort 10 mg filmsko obložene tablete
Citafort 15 mg filmsko obložene tablete
Citafort 20 mg filmsko obložene tablete

Sweden: Escitalopram Sandoz