Showing 12 authorised medicines
Medicine Active substance Licence holder Status
Efavirenz/Emtricitabine/Tenofovir disoproxil Teva 600 mg/200 mg/245 mg Film-coated Tablets PA1986/033/001
Efavirenz, Emtricitabine, Tenofovir disoproxil
Teva B.V.
Marketed
Emtricitabine/Tenofovir disoproxil Accordpharma 200 mg/245 mg film-coated tablets PA2315/200/002
Emtricitabine, Tenofovir disoproxil
Accord Healthcare Ireland Ltd.
Marketed
Emtricitabine/Tenofovir disoproxil Krka 200 mg/245 mg film-coated tablets EU/1/16/1151/001-004
Emtricitabine, Tenofovir disoproxil
KRKA, d.d., Novo mesto
—
Emtricitabine/Tenofovir disoproxil Krka d.d 200 mg/245 mg film-coated tablets EU/1/17/1182/001-004
Tenofovir disoproxil, Emtricitabine
KRKA, d.d., Novo mesto
—
Emtricitabine/Tenofovir disoproxil Mylan 200 mg/245 mg film-coated tablets EU/1/16/1133/001-006
Emtricitabine, Tenofovir disoproxil
Mylan Pharmaceuticals Limited
—
Emtricitabine/Tenofovir disoproxil Teva 200 mg/245 mg film-coated tablets PA1986/016/001
Emtricitabine, Tenofovir disoproxil
Teva B.V.
Marketed
Emtricitabine/Tenofovir disoproxil Tillomed 200 mg/245 mg film-coated tablets PA22720/008/001
Emtricitabine, Tenofovir disoproxil
Tillomed Pharma GmbH
Not marketed
Emtricitabine/Tenofovir disoproxil Zentiva 200 mg/245 mg film-coated tablets EU/1/16/1148/001-002
Tenofovir disoproxil, Emtricitabine
Zentiva k.s.
—
Stribild 150 mg/150 mg/200 mg/245 mg film-coated tablets EU/1/13/830/001
Emtricitabine, Tenofovir disoproxil, Cobicistat, Elvitegravir
Gilead Sciences Ireland UC
—
Tenofovir Disoproxil Teva 245 mg film-coated tablets PA1986/003/001
Tenofovir disoproxil
Teva B.V.
Marketed
Tenofovir disoproxil Viatris 245 mg film-coated tablets EU/1/16/1129/001
Tenofovir disoproxil
Viatris Limited
—
Truvada 200 mg/245 mg film-coated tablets EU/1/04/305/001-002
Emtricitabine, Tenofovir disoproxil
Gilead Sciences Ireland UC
—
Cite this database
Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 6 July 2026).
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Data: Health Products Regulatory Authority (HPRA) open dataset (“Authorised or Transfer Pending Products”), licensed CC BY 4.0, refreshed daily. Regulatory information only — not medical advice.