Patient leaflet - LEVODOPA/CARBIDOPA/ENTACAPONE MYLAN 100 MG / 25 MG / 200 MG FILM-COATED TABLETS
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
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– Keep this leaflet. You may need to read it again.
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– If you have any further questions, ask your doctor or pharmacist.
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– This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
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– If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.
What is in this leaflet
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1. What Levodopa/Carbidopa/Entacapone is and what it is used for
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2. What you need to know before you take Levodopa/Carbidopa/Entacapone
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3. How to take Levodopa/Carbidopa/Entacapone
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4. Possible side effects
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5. How to store Levodopa/Carbidopa/Entacapone
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6. Contents of the pack and other information
1. what levodopa/carbidopa/entacapone is and what it is used for
Levodopa/Carbidopa/Entacapone contains three active substances (levodopa, carbidopa and entacapone) in one film-coated tablet. Levodopa/Carbidopa/Entacapone is used for the treatment of Parkinson’s disease.
Parkinson’s disease is caused by low levels of a substance called dopamine in the brain. Levodopa increases the amount of dopamine and hence reduces the symptoms of Parkinson’s disease. Carbidopa and entacapone improve the antiparkinson effects of levodopa.
2. what you need to know before you take levodopa/carbidopa/entacapone- are allergic to levodopa, carbidopa entacapone, or any of the other ingredients of this medicine (listed in section 6)
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– have narrow-angle glaucoma (an eye disorder)
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– have a tumour of the adrenal gland
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– are taking certain medicines for treating depression (combinations of selective MAO-A and
MAO-B inhibitors, or non-selective MAO-inhibitors e.g. phenelzine, tranylcypromine)
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– have ever had neuroleptic malignant syndrome (NMS – this is a rare reaction to medicines used to treat severe mental disorders)
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– have ever had non-traumatic rhabdomyolysis (a rare muscle disorder)
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– have a severe liver disease.
Warnings and precautions
Talk to your doctor or pharmacist before taking Levodopa/Carbidopa/Entacapone if you have or have ever had:
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– a heart attack or any other diseases of the heart including cardiac arrythmias, or of the blood vessels
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– asthma or any other disease of the lungs
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– a liver problem, because your dose may need to be adjusted
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– kidney or hormone-related diseases
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– stomach ulcers or convulsions
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– any form of serious mental health issue like psychosis
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– chronic wide-angle glaucoma, because your dose may need to be adjusted and the pressure in your eyes may need to be monitored.
Consult your doctor if you are currently taking:
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– antipsychotics (medicines used to treat psychosis)
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– a medicine which may cause low blood pressure when rising from a chair or bed.
You should be aware that Levodopa/Carbidopa/Entacapone may make these reactions worse.
Consult your doctor if during the treatment with Levodopa/Carbidopa/Entacapone you:
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– notice that your muscles get very rigid or jerk violently, or if you get tremors, agitation, confusion, fever, rapid pulse, or wide fluctuations in your blood pressure. If any of this happens, contact your doctor immediately
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– feel depressed, have suicidal thoughts, or notice unusual changes in your behaviour
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– find yourself suddenly falling asleep, or if you feel very drowsy. If this happens, you should not drive or use any tools or machines (see also section ‚Driving and using machines‘)
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– notice that uncontrolled movements begin or get worse after you started to take Levodopa/Carbidopa/Entacapone. If this happens, your doctor may need to change the dose of your antiparkinson medicine
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– experience diarrhoea: monitoring of your weight is recommended in order to avoid potentially excessive weight loss
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– if you experience prolonged diarrhoea consult your doctor as it may be a sign of inflammation of the colon
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– experience progressive anorexia (loss of appetite), asthenia (weakness, exhaustion) and weight decrease within a relatively short period of time. This may be a sign of problems with your liver and your doctor may wish to carry out tests.
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– feel the need to stop using Levodopa/Carbidopa/Entacapone, see section ‚If you stop taking Levodopa/Carbidopa/Entacapone ‘.
Tell your doctor if you or your family/carer notices you are developing addiction-like symptoms leading to craving for large doses of [Nationally completed name] and other medicines used to treat Parkinson’s disease.
Tell your doctor if you or your family/carer notices you are developing urges or cravings to behave in ways that are unusual for you or you cannot resist the impulse, drive or temptation to carry out certain activities that could harm yourself or others. These behaviours are called impulse control disorders and can include addictive gambling, excessive eating or spending, an abnormally high sex drive or a preoccupation with an increase in sexual thoughts or feelings. Your doctor may need to review your treatments.
Your doctor may take some regular laboratory tests during a long term treatment with Levodopa/Carbidopa/Entacapone.
If you must undergo surgery, please tell your doctor that you are using Levodopa/Carbidopa/Entacapone.
Levodopa/Carbidopa/Entacapone is not recommended to be used for treatment of extrapyramidal symptoms (e.g. involuntary movements, shaking, muscle rigidity and muscle contractions) caused by other medicines.
Children and adolescents
Experience with Levodopa/Carbidopa/Entacapone in patients under 18 years is limited. Therefore, the use of Levodopa/Carbidopa/Entacapone in children is not recommended.
Other medicines and Levodopa/Carbidopa/Entacapone
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription and herbal medicines.
Do not take Levodopa/Carbidopa/Entacapone if you are taking certain medicines for treating depression (combinations of selective MAO-A and MAO-B inhibitors, or non-selective MAO inhibitors) e.g. phenelzine, tranylcypromine) (see above “Do not take Levodopa/Carbidopa/Entacapone if you”).
Levodopa/Carbidopa/Entacapone may increase the effects and side effects of certain medicines. These include:
- medicines used to treat depression such as moclobemide, amitryptiline, desipramine, maprotiline, venlafaxine and paroxetine
- medicines used to treat high blood pressure
The effects of levodopa/carbidopa/entacapone may be weakened by certain medicines. These include:
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– dopamine antagonists used to treat mental health conditions , or prevent nausea (feeling sick) and vomiting (being sick)
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– phenytoin, used to prevent convulsions
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– papaverine used to relax the muscles.
Levodopa/carbidopa/entacapone may make it harder for you to digest iron. Therefore, do not take Levodopa/Carbidopa/Entacapone and iron supplements at the same time. After taking one of them, wait at least 2 to 3 hours before taking the other.
Levodopa/Carbidopa/Entacapone with food and drink
Levodopa/Carbidopa/Entacapone may be taken with or without food. For some patients, levodopa/carbidopa/entacapone may not be well absorbed if it is taken with, or shortly after eating protein-rich food (such as meats, fish, dairy products, seeds and nuts). Consult your doctor if you think this applies to you.
Pregnancy and breast-feeding
Pregnancy
If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Levodopa/Carbidopa/Entacapone is not recommended during pregnancy unless the benefits for the mother outweigh the possible risks to the baby.
Breast-feeding
You should not breast-feed during treatment with Levodopa/Carbidopa/Entacapone.
Driving and using machines
Levodopa/carbidopa/entacapone may lower your blood pressure, which may make you feel lightheaded or dizzy. Therefore, be particularly careful when you drive or when you use any tools or machines.
If you feel very drowsy, or if you sometimes find yourself suddenly falling asleep, wait until you feel fully awake again before driving or doing anything else that requires you to be alert. Otherwise, you may put yourself and others at risk of serious injury or death.
Levodopa/Carbidopa/Entacapone contains lactose and sodium
If you have been told by your doctor that you have intolerance to some sugars, contact your doctor before taking this medicine.
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.
3. how to take levodopa/carbidopa/entacapone
Always take this medicine exactly as your doctor or pharmacist has told you. You should check with your doctor or pharmacist if you are not sure.
For adults and elderly:
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– Your doctor will tell you exactly how many tablets of Levodopa/Carbidopa/Entacapone to take each day.
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– The tablets are not intended to be split or broken into smaller pieces.
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– You should take only one tablet each time.
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– Depending on how you respond to treatment, your doctor may suggest a higher or lower dose.
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– Levodopa/Carbidopa/Entacapone may be taken with or without food. For some patients, this medicine may not be well absorbed if it is taken with, or shortly after eating protein-rich food (see section 2 “Levodopa/Carbidopa/Entacapone with food and drink”).
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– If you are taking Levodopa/Carbidopa/Entacapone 50 mg/12.5 mg/200 mg, 75 mg/18.75 mg/200 mg, 100 mg/25 mg/200 mg, 125 mg/31.25 mg/200 mg or 150 mg/37.5 mg/200 mg tablets, do not take more than 10 tablets per day.
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– If you are taking Levodopa/Carbidopa/Entacapone 175mg/43.75mg/200mg tablets, do not take more than 8 tablets per day.
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– If you are taking Levodopa/Carbidopa/Entacapone 200 mg/50 mg/200mg tablets, do not take more than 7 tablets per day.
Talk to your doctor or pharmacist if you think the effect of Levodopa/Carbidopa/Entacapone is too strong or too weak, or if you experience possible side effects
If you take more Levodopa/Carbidopa/Entacapone than you should
If you have accidentally taken more Levodopa/Carbidopa/Entacapone tablets than you should, talk to your doctor or pharmacist immediately. In case of an overdose you may experience changes in your breathing, feel confused or agitated, your heart rate may be slower or faster than normal or the color of your skin, tongue, eyes or urine may change.
If you forget to take Levodopa/Carbidopa/Entacapone
Do not take a double dose to make up for a forgotten tablet.
If it is more than 1 hour until your next dose:
Take one tablet as soon as you remember, and the next tablet at the normal time.
If it is less than 1 hour until your next dose:
Take a tablet as soon as you remember, wait 1 hour, then take another tablet. After that carry on as normal.
Always leave at least an hour between Levodopa/Carbidopa/Entacapone tablets, to avoid possible side effects.
If you stop taking Levodopa/Carbidopa/Entacapone
Do not stop taking Levodopa/Carbidopa/Entacapone unless your doctor tells you to. In such a case your doctor may need to adjust your other antiparkinson medicines, especially levodopa, to give sufficient control of your symptoms. If you suddenly stop taking Levodopa/Carbidopa/Entacapone and other antiparkinsonian medicines it may result in unwanted side effects.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
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Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them. If you experience any of these side effects, talk to your doctor as soon as possible. Many of the side effects can be relieved by adjusting the dose.
If you during the treatment with Levodopa/Carbidopa/Entacapone you experience the following symptoms, contact your doctor immediately or go to the nearest hospital casualty department straight away :
Common (may affect up to 1 in 10 people)
- heart condition which can cause chest pain (angina pectoris), shortness of breath and swelling of the feet or legs due to fluid retention
Uncommon (may affect up to 1 in 100 people)
- heart attack. You may experience severe chest pain, tingling or feeling clammy
- bleeding in the gut. You may become sick and notice blood or you pass stools which are bloody or black
Rare (may affect up to 1 in 1,000 people)
- serious allergic reaction, the signs may include hives (nettle rash), itching, rash, swelling of your
face, lips, tongue or throat. This may cause difficulties in breathing or swallowing.
Not known (cannot be estimated from the available data)
- your muscles get very rigid or jerk violently, you get tremors, agitation, confusion, fever, rapid pulse, or wide fluctuations in your blood pressure or red-brown discoloration of the urine due to destruction of muscle fibres. These can be symptoms of neuroleptic malignant syndrome (NMS, a rare severe reaction to medicines used to treat disorders of the central nervous system) or rhabdomyolysis (a rare severe muscle disorder)
- fits (convulsions)
- suicidal thoughts or behaviour
Tell your doctor straight away, if you experience any of the following:
Common (may affect up to 1 in 10 people)
- suddenly falling asleep
Uncommon (may affect up to 1 in 100 people)
- severe mental condition in which you lose contact with reality and is unable to think and judge
clearly
- difficulty passing urine or emptying the bladder
Not known (cannot be estimated from the available data)
- depression
- yellowing of the whites of the eyes or skin, dark urine, pale coloured bowel movements, itching due to problems with your liver
- inability to resist the impulse to perform an action that could be harmful, which may include:
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– strong impulse to gamble excessively despite serious or personal family consequences
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– altered or increased sexual interest and behaviour of significant concern to you or to others, for example, an increased sexual drive
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– uncontrollable excessive shopping or spending
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– binge eating (eating large amounts of food in a short time period) or compulsive eating (eating more food than normal and more than is needed to satisfy your hunger).
Tell your doctor if you experience any of these behaviours; they will discuss ways of managing or reducing the symptoms.
Other possible side effects
Very common (may affect more than 1 in 10 people)
- uncontrolled movements (dyskinesias)
- feeling sick (nausea)
- harmless reddish-brown discolouration of urine
- muscle pain
- diarrhoea
Common (may affect up to 1 in 10 people)
- light-headedness or fainting due to low blood pressure, high blood pressure
- worsening of Parkinson's symptoms, such as slow or instable movement, shaking, uncontrollable muscle spasms affecting the eyes, head, neck and body, loss of memory
- dizziness, drowsiness
- vomiting, abdominal pain and discomfort, heartburn, dry mouth, constipation
- inability to sleep
- seeing, feeling or hearing things that are not (hallucinations), confusion, abnormal dreams (including nightmares)
- tiredness or unusual weakness
- mental changes – including problems with memory and anxiety heart or artery disease events (e.g. chest pain), irregular heart rate or rhythm
- more frequent falling
- shortness of breath
- increased sweating
- rash
- muscle cramps
- swelling of legs
- disturbances in the manner of walking
- blurred vision
- a reduction in the number of red blood cells (anaemia)
- decreased appetite, decreased weight
- headache
- joint pain
- urinary tract infection
Uncommon (may affect up to 1 in 100 people)
- changes in the blood cell count which may result in bleeding or bruising for longer than normal or unexpectedly due to reduced number of platelets, abnormal liver function tests seen in a blood test
- feeling agitated
- inflammation of the colon (colitis) which may cause persistent stomach cramps and diarrhoea discolourations other than urine (e.g. skin, nail, hair, sweat) swallowing difficulties
generally feeling unwell
Not known (cannot be estimated from the available data)
- _itchy red rash
- craving for large doses of [Nationally completed name] in excess of that required to control motor symptoms, known as dopamine dysregulation syndrome. Some patients experience severe abnormal involuntary movements (dyskinesias), mood swings or other side effects after taking large doses of levodopa/carbidopa/entacapone.
Reporting of side effects
If you get any side effects talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at
By reporting side effects you can help provide more information on the safety of this medicine.
5. how to store levodopa/carbidopa/entacapone
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 bottle and the carton after EXP.
The expiry date refers to the last day of that month.
Shelf life after first opening the container: 3 months
Store below 25°C.
Only for blistered product: Store in the original package in order to protect from moisture
Only for bottle product: Store in the original packaging and keep the bottle tightly closed in order to protect from moisture.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
6. contents of the pack and other information- the active substances are levodopa, carbidopa and entacapone.
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– Each film-coated tablet contains 50 mg of levodopa, 12.5 mg of carbidopa anhydrous (as 13.5mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 75 mg of levodopa, 18.75 mg of carbidopa anhydrous (as 20.24 mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 100 mg of levodopa, 25 mg of carbidopa anhydrous (as 27 mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 125 mg of levodopa, 31.25 mg of carbidopa anhydrous (as 33.74 mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 150 mg of levodopa, 37.5 mg of carbidopa anhydrous (as 40.48 mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 175 mg of levodopa, 43.75 mg of carbidopa anhydrous (as 47.23 mg carbidopa monohydrate) and 200 mg of entacapone.
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– Each film-coated tablet contains 200 mg of levodopa, 50 mg of carbidopa anhydrous (as 54 mg carbidopa monohydrate) and 200 mg of entacapone.
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– The other ingredients in the tablet core are croscarmellose sodium (E468), cellulose microcrystalline E460, poloxamer 188, hydroxypropyl cellulose (E463), lactose monohydrate
(see section 2 ‘[Levodopa/Carbidopa/Entacapone 50 mg/12.5 mg/200 mg, 75 mg/18.75 mg/200 mg, 100 mg/25 mg/200 mg, 125 mg/31.25 mg/200 mg or 150 mg/37.5 mg/200 mg tablets] contains lactose’), magnesium stearate (E470b).
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– The ingredients in the film-coating are
What Levodopa/Carbidopa/Entacapone looks like and contents of the pack
Levodopa/Carbidopa/Entacapone 50 mg/12.5 mg/200 mg film-coated tablets: brownish red colored, round shaped, biconvex, film-coated tablets debossed '50’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 75 mg/18.75 mg/200mg film-coated tablets: light brownish red colored, oval shaped, biconvex, film coated tablets debossed “75” on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 100 mg/25 mg/200 mg film-coated tablets: brownish red colored, oval, shaped, biconvex, film-coated tablets debossed ' 100’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 125 mg/31.25 mg/200 mg film-coated tablets: light brownish red colored, oval shaped, biconvex, film-coated tablets debossed '125’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 150 mg/37.5 mg/200 mg film-coated tablets: brownish red colored, oval shaped, biconvex, film-coated tablets debossed ' 150’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 175 mg/43.75 mg/200 mg film-coated tablets: light brownish red colored, oval shaped, biconvex, film-coated tablets debossed '175’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone 200 mg/50 mg/200 mg film-coated tablets: dark brownish red colored, oval shaped, biconvex, film-coated tablets debossed '200’ on one side and plain on the other side.
Levodopa/Carbidopa/Entacapone comes in different pack sizes as HDPE bottle with an Aluminium Induction Seal -Cap and Silica Gel Canister (as a loose component) in the HDPE bottle and Blister (Aluminium-Aluminium) containing 30 or 100 tablets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Generics [UK] Limited, Potters Bar, Hertfordshire, EN6 1TL, U.K.
Manufacturer
Wessling Hungary Kft, Budapest, Foti ut.56. 1047, Hungary
Mylan Hungary Kft, H-2900 Komarom, Mylan utca, Hungary
This leaflet was last revised in 09/2020