Package Leaflet: Information for the Patient
Lercanidipine Sandoz10 mg film-coated tablets EFG
Lercanidipine Sandoz20 mg film-coated tablets EFG
lercanidipine hydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Lercanidipine Sandoz, lercanidipine hydrochloride, belongs to a group of medicines called calcium channel blockers (of the dihydropyridine type) that lower blood pressure.
Lercanidipine is used to treat high blood pressure, also known as arterial hypertension, in adults over 18 years old (it is not recommended for children and adolescents under 18 years of age).
Do not take Lercanidipine Sandoz:
Do not take this medicine if you are pregnant or breastfeeding, or if you wish to become pregnant or are of childbearing age and not using contraceptive methods (for more information, see section Pregnancy, breastfeeding and fertility).
Warnings and precautions
Consult your doctor or pharmacist before starting to take lercanidipine:
Children and adolescents
The safety and efficacy of lercanidipine have not been established in children and adolescents under 18 years of age.
Taking Lercanidipine Sandoz with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
It is especially important that you tell your doctor if you are being treated with any of the following medicines:
Taking Lercanidipine Sandoz with food, drinks and alcohol
Pregnancy, breastfeeding and fertility
Do not take lercanidipine if you are pregnant or breastfeeding, or if you wish to become pregnant or are of childbearing age and not using contraceptive methods.
Consult your doctor or pharmacist before using this medicine.
Driving and using machines
Be cautious as dizziness, weakness, fatigue and rarely somnolence may occur. Do not drive or use machines until you know how lercanidipine affects you.
Lercanidipine Sandoz contains lactose and sodium
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult with them before taking this medicine.
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially "sodium-free".
Follow exactly the instructions of administration of this medicine indicated by your doctor. In case of doubt, ask your doctor or pharmacist.
Adults
The recommended dose is one 10 mg Lercanidipine tablet per day, taken always at the same time each day, preferably in the morning, at least 15 minutes before breakfast, as a fatty meal significantly increases the levels of this medicine in the blood.
Your doctor will indicate, if necessary, to increase the dose to one 20 mg Lercanidipine tablet per day.
The tablets should be swallowed whole with a little water. The score line is only to facilitate breaking and swallowing, but not to divide into equal doses.
Lercanidipine is not recommended for use in children and adolescents under 18 years of age.
Elderly
No dose adjustment is required. However, they may require special care at the start of treatment.
Patients with kidney or liver problems
Special care is needed at the start of treatment in these patients and an increase in dose to 20 mg per day should be done with caution.
Use in children and adolescents
This medicine should not be given to children and adolescents under 18 years of age.
If you take more Lercanidipine Sandoz than you should
Do not take more than the prescribed dose.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicine and the amount ingested.
If you take more than the prescribed dose or in case of overdose, seek medical attention immediately and, if possible, take your tablets and/or packaging with you.
Exceeding the recommended dose may cause your blood pressure to drop too low and your heart rate to become irregular or faster, you may feel dizzy or have a headache.
If you forget to take Lercanidipine Sandoz
If you have forgotten to take your tablet, simply omit the forgotten dose and take the next one when it is due.
Do not take a double dose to make up for forgotten doses.
If you stop taking Lercanidipine Sandoz
If you stop taking lercanidipine, your blood pressure will rise again. Consult your doctor before stopping the medicine.
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.
Some of these side effects can be serious:
If you experience any of these side effects, tell your doctor immediately.
Rare (may affect up to 1 in 1,000 people):
Chest pain (angina), fainting and allergic reactions (with symptoms including itching, rash and hives, difficulty breathing or swelling, dizziness).
If you have pre-existing angina, with medicines of the group to which lercanidipine belongs, you may experience an increase in frequency, duration or severity of these attacks. Isolated cases of heart attacks have been observed.
Frequency not known (cannot be estimated from the available data):
Swelling of the face, lips, tongue or throat that may cause difficulty breathing or swallowing.
Other possible side effects:
Common (may affect up to 1 in 10 people)
Headache, increased heart rate, palpitations (heartbeats or acceleration), flushing (e.g. in the face), swelling of the ankles.
Uncommon (may affect up to 1 in 100 people)
Dizziness, low blood pressure, indigestion, discomfort, stomach pain, rash, itching, muscle pain, production of large amounts of urine, weakness or fatigue.
Rare (may affect up to 1 in 1,000 people):
Somnolence, discomfort, diarrhea, blisters, increased frequency of urination, chest pain.
Frequency not known (cannot be estimated from the available data):
Gingival inflammation, changes in liver function (detected in blood tests); cloudy liquid (when dialysis is performed through a tube inside the abdomen).
Reporting of side effects
If you experience 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 Spanish Pharmacovigilance System for Human Use Medicines: https://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 carton, after EXP. The expiry date is the last day of the month stated.
Aluminium/PVC blister: Do not store above 25°C.
Store in the original package to protect from moisture.
Aluminium/PVDC blister: Do not store above 25°C.
Store in the original package to protect from moisture.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to a pharmacy. Ask your pharmacist how to dispose of medicines no longer required. This will help to protect the environment.
Composition of Lercanidipine Sandoz
Each 10 mg Lercanidipine Sandoz film-coated tablet contains 10 mg of lercanidipine hydrochloride, equivalent to 9.4 mg of lercanidipine.
Each 20 mg Lercanidipine Sandoz film-coated tablet contains 20 mg of lercanidipine hydrochloride, equivalent to 18.8 mg of lercanidipine.
Core of the tablet:magnesium stearate, povidone, sodium carboxymethylcellulose (type A), lactose monohydrate, microcrystalline cellulose.
Lercanidipine Sandoz 10 mg:
Coating:macrogol, partially hydrolyzed polyvinyl alcohol, talc, titanium dioxide (E 171), yellow iron oxide (E 172).
Lercanidipine Sandoz 20 mg:
Coating:macrogol, partially hydrolyzed polyvinyl alcohol, talc, titanium dioxide (E 171), yellow iron oxide (E 172), red iron oxide (E 172).
Appearance of the product and contents of the pack
Lercanidipine Sandoz 10 mg: yellow, round, biconvex film-coated tablets, 6.5 mm in diameter, scored on one side and marked with "L" on the other.
Lercanidipine Sandoz 20 mg: pink, round, biconvex film-coated tablets, 8.5 mm in diameter, scored on one side and marked with "L" on the other.
The score line is only to facilitate breaking and swallowing, but not to divide into equal doses.
Pack sizes:
Lercanidipine Sandoz 10 mg: 7, 10, 14, 20, 28, 30, 35, 50, 56, 60, 98 and 100 film-coated tablets.
Lercanidipine Sandoz 20 mg: 7, 10, 14, 20, 28, 30, 35, 42, 50, 56, 60, 98 and 100 film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
Marketing authorisation holder
Sandoz Farmacéutica, S.A.
Centro Empresarial Parque Norte
Edificio Roble
C/ Serrano Galvache, 56
28033 Madrid
Spain
Manufacturer
Salutas Pharma GmbH
Otto von Guericke Allee 1
39179 Barleben
Germany
Or
Balkanpharma-Dupnitsa AD,
3 Samokovsko Shosse Str.
Dupnitza 2600
Bulgaria
Or
ACTAVIS LIMITED.
BLB016 Bulebel Industrial Estate
Zejtun ZTN3000
Malta
Or
Lek Pharmaceuticals d.d.
Verovskova 57
SI-1526 Ljubljana
Slovenia
This medicine is authorised in the Member States of the European Economic Area under the following names:
Austria: Lercanidipin Sandoz 10 mg – Filmtabletten
Lercanidipin Sandoz 20 mg – Filmtabletten
Belgium: Lercanidipin Sandoz 10 mg filmomhulde tabletten
Lercanidipin Sandoz 20 mg filmomhulde tabletten
Denmark: Lercatio
Italy: Lercanidipina Sandoz
Netherlands: Lercanidipine HCl Sandoz 10 mg, filmomhulde tabletten
Lercanidipine HCl Sandoz 20 mg, filmomhulde tabletten
Portugal: Lercanidipina Sandoz
Date of last revision of this leaflet:June 2020.
Detailed 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 LERCANIDIPINE SANDOZ 20 mg FILM-COATED TABLETS in October, 2025 is around 12.47 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.