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Buplex 400mg film-coated tablets



Teva B.V.PA1986/116/002

Main Information

Trade NameBuplex 400mg film-coated tablets
Active SubstancesIbuprofen
Dosage FormFilm-coated tablet
Licence HolderTeva B.V.
Licence NumberPA1986/116/002

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 LicenceProduct not subject to medical prescription, supply through pharmacies only and promotion to the public subject to the following restrictions: maximum strength 400 mg, maximum pack size 25, maximum dose 400 mg, maximum daily dose 1200 mg, limited indications. For use in adults and children not under 12 years.
Marketing StatusMarketed

Documents

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