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Ibuprofen Farmalider 200 mg film-coated tablets



Farmalider, S.A.PA2090/002/001

Main Information

Trade NameIbuprofen Farmalider 200 mg film-coated tablets
Active SubstancesIBUPROFEN PH. EUR.
Dosage FormFilm-coated tablet
Licence HolderFarmalider, S.A.
Licence NumberPA2090/002/001

Group Information

ATC CodeM01AE Propionic acid derivatives
M01AE01 ibuprofen

Status

License statusAuthorised
Licence Issued05/01/2018
Legal statusProduct not subject to medical prescription
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to the general public
Conditions of LicenceSupply through pharmacies and promotion to the public only if compliant with the following restrictions: maximum strength: 200 mg; maximum pack size 50; maximum dose: 400 mg; maximum daily dose 1200 mg; limited indications.
Marketing StatusNot marketed

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
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