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Buplex 200mg film-coated tablets



Teva B.V.PA1986/116/001

Main Information

Trade NameBuplex 200mg film-coated tablets
Active SubstancesIbuprofen
Dosage FormFilm-coated tablet
Licence HolderTeva B.V.
Licence NumberPA1986/116/001

Group Information

ATC CodeM01AE Propionic acid derivatives
M01AE01 ibuprofen

Status

License statusAuthorised
Licence Issued03/07/2009
Legal statusProduct not subject to medical prescription
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to the general public
Conditions of LicenceSupply through pharmacies only and promotion to the public subject the the following restrictions: maximum strength 200 mg, maximum pack size 50, maximum dose 400mg, maximum daily dose 1200 mg, limited indications.
Marketing StatusMarketed

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportPDF Version
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