Buplex 200mg film-coated tablets

Licence status
Authorised: 03/07/2009
Active substances
Ibuprofen
Dosage Form
Film-coated tablet
Licence number
PA1986/116/001
Licence holder
Teva B.V.

Product documents

Licence information

ATC code
M01AE Propionic acid derivatives, M01AE01 ibuprofen
Legal supply status
Product not subject to medical prescription
Place of sale
Supply through pharmacies only
Conditions of Licence
Subject to the following restriction: maximum strength 200 mg, maximum pack size 50, maximum dose: 400 mg, maximum daily dose 1200 mg, limited indications.
Marketing availability
Marketed
Advertising conditions
Advertising to the general public
Licence issued
03/07/2009