The HPRA advises healthcare professionals not to retain printed versions of Summary of Product Characteristics (SPC) documents. As these documents are subject to frequent content updates, including changes to safety and dose related information, we recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about specific SPCs on our website then please e-mail info@hpra.ie


REYATAZ

50 Milligram Oral Powder

Bristol Myers Squibb Pharma EEIGEU/1/03/267/012

Main Information

Trade NameREYATAZ
Active SubstancesATAZANAVIR SULFATE
Strength50 Milligram
Dosage FormOral Powder
Licence HolderBristol Myers Squibb Pharma EEIG
Licence NumberEU/1/03/267/012

Group Information

ATC CodeJ05AE08 atazanavir

Status

Authorised/WithdrawnAuthorised
Licence Issued21/06/2016
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceMedicinal product subject to restricted medical prescription (see Annex I: Summary of Product Characteristics, section 4.2).
Marketing Status

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website
« Back