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Entacapone Teva
entacapone

Package leaflet: information for the user


Entacapone Teva 200 mg film-coated tablets

entacapone


Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.


Tell your doctor if you experience any of these behaviours; they will discuss ways of managing or

reducing the symptoms.


Reporting of side effects

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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. You can also report side effects directly via the national reporting system listed in Appendix V. By reporting side effects you can help provide more information on the safety of

this medicine.


  1. How to store Entacapone Teva


    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 and tablet container label after EXP. The expiry date refers to the last day of that month.

    This medicinal product does not require any special storage conditions.


    Do not throw away any medicines via wastewater. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.


  2. Contents of the pack and other information What Entacapone Teva contains


What Entacapone Teva looks like and contents of the pack

Entacapone Teva film-coated tablets are light brown, biconvex ellipse-shaped with approximately 18 mm length and 10 mm width, embossed with “E200” on one side and plain on the other side.


Entacapone Teva is available in HDPE tablet containers with polypropylene screw caps with desiccant insert containing 30, 60, 100 or 175 film-coated tablets. Not all pack sizes may be marketed.


Marketing Authorisation Holder

Teva B.V. Swensweg 5 2031GA Haarlem The Netherlands


Manufacturer

TEVA Pharmaceutical Works Private Limited Company

Pallagi út 13,

4042 Debrecen, Hungary


Pharmachemie B.V. Swensweg 5,

2031 GA Haarlem, The Netherlands


Teva Czech Industries s.r.o. Ostravska 29, c.p. 305,

74770 Opava-Komarov, Czech Republic


Teva Operations Poland Sp.z.o.o ul. Mogilska 80,

31-546, Krakow,

Poland


For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:


België/Belgique/Belgien

Teva Pharma Belgium N.V./S.A./AG Tél/Tel: +32 38207373

Lietuva

UAB Teva Baltics Tel: +370 52660203

България

Тева Фарма ЕАД Teл: +359 24899585

Luxembourg/Luxemburg ratiopharm GmbH Allemagne/Deutschland Tél/Tel: +49 73140202


Česká republika

Teva Pharmaceuticals CR, s.r.o. Tel: +420 251007111

Magyarország

Teva Gyógyszergyár Zrt. Tel: +36 12886400


Danmark

Teva Denmark A/S

Tlf: +45 44985511

Malta

Teva Pharmaceuticals Ireland

L-Irlanda

Tel: +44 2075407117


Deutschland

TEVA GmbH

Tel: +49 73140208

Nederland

Teva Nederland B.V. Tel: +31 8000228400


Eesti

UAB Teva Baltics Eesti filiaal Tel: +372 6610801

Norge

Teva Norway AS Tlf: +47 66775590


Ελλάδα

Specifar Α.Β.Ε.Ε. Τηλ: +30 2118805000

Österreich

ratiopharm Arzneimittel Vertriebs-GmbH Tel: +43 1970070


España

Teva Pharma, S.L.U. Tel: +34 913873280

Polska

Teva Pharmaceuticals Polska Sp. z o.o. Tel: +48 223459300


France

Teva Santé

Tél: +33 155917800

Portugal

Teva Pharma - Produtos Farmacêuticos, Lda. Tel: +351 214767550


Hrvatska

Pliva Hrvatska d.o.o.

Tel: +385 13720000

România

Teva Pharmaceuticals S.R.L. Tel: +40 212306524


Ireland

Teva Pharmaceuticals Ireland Tel: +44 2075407117

Slovenija

Pliva Ljubljana d.o.o. Tel: +386 15890390


Ísland

Teva Pharma Iceland ehf. Sími: +354 5503300

Slovenská republika

TEVA Pharmaceuticals Slovakia s.r.o. Tel: +421 257267911


Italia

Teva Italia S.r.l. Tel: +39 028917981

Suomi/Finland

Teva Finland Oy

Puh/Tel: +358 201805900


Κύπρος

Specifar Α.Β.Ε.Ε. Ελλάδα

Τηλ: +30 2118805000

Sverige

Teva Sweden AB Tel: +46 42121100


Latvija

UAB Teva Baltics filiāle Latvijā

Tel: +371 67323666

United Kingdom (Northern Ireland)

Teva Pharmaceuticals Ireland Ireland

Tel: +44 2075407117


This leaflet was last revised in MM/YYYY.


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