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Lamivudine/Zidovudine Teva



Teva Pharma B.V.EU/1/10/663/001-002

Main Information

Trade NameLamivudine/Zidovudine Teva
Active SubstancesZidovudine
Lamivudine
Dosage FormFilm-coated tablet
Licence HolderTeva Pharma B.V.
Licence NumberEU/1/10/663/001-002

Group Information

ATC CodeJ05A DIRECT ACTING ANTIVIRALS

Status

License statusWithdrawn
Withdrawn Date09/03/2023
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 StatusUnknown

Documents

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